Article

Article - Ankle-Foot/Knee-Ankle-Foot Orthoses - Policy Article

(A52457)
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Contractor Information
CONTRACTOR NAME CONTRACT TYPE CONTRACT JURISDICTION STATES
NUMBER

CGS Administrators, LLC DME MAC 17013 - DME MAC J-B Illinois
Indiana
Kentucky
Michigan
Minnesota
Ohio
Wisconsin

CGS Administrators, LLC DME MAC 18003 - DME MAC J-C Alabama
Arkansas
Colorado
Florida
Georgia
Louisiana
Mississippi
New Mexico
North Carolina
Oklahoma
Puerto Rico
South Carolina
Tennessee
Texas
Virgin Islands
Virginia
West Virginia

Noridian Healthcare Solutions, DME MAC 16013 - DME MAC J-A Connecticut
LLC Delaware
District of Columbia
Maine
Maryland
Massachusetts
New Hampshire
New Jersey
New York - Entire State
Pennsylvania
Rhode Island
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CONTRACTOR NAME CONTRACT TYPE CONTRACT JURISDICTION STATES
NUMBER

Vermont

Noridian Healthcare Solutions, DME MAC 19003 - DME MAC J-D Alaska
LLC American Samoa
Arizona
California - Entire State
Guam
Hawaii
Idaho
Iowa
Kansas
Missouri - Entire State
Montana
Nebraska
Nevada
North Dakota
Northern Mariana
Islands
Oregon
South Dakota
Utah
Washington
Wyoming

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Ankle-Foot/Knee-Ankle-Foot Orthoses - Policy Article AMA is not recommending their use. The AMA does not directly or indirectly
practice medicine or dispense medical services. The AMA assumes no
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Current Dental Terminology © 2024 American Dental Association. All rights
Article
reserved.

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Created on 02/13/2025. Page 2 of 29
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Article Guidance
Article Text

NON-MEDICAL NECESSITY COVERAGE AND PAYMENT RULES

For any item to be covered by Medicare, it must 1) be eligible for a defined Medicare benefit category, 2) be
reasonable and necessary for the diagnosis or treatment of illness or injury or to improve the functioning of a
malformed body member, and 3) meet all other applicable Medicare statutory and regulatory requirements.
Information provided in this policy article relates to determinations other than those based on Social Security Act
§1862(a)(1)(A) provisions (i.e. “reasonable and necessary”).

For a beneficiary’s orthosis to be eligible for reimbursement the reasonable and necessary (R&N) requirements set
out in the related Local Coverage Determination must be met. In addition, there are specific statutory payment policy
requirements, discussed below, that also must be met.

Ankle-foot orthoses (AFO) and knee-ankle-foot orthoses (KAFO) are covered under the Medicare braces benefit
(Social Security Act §1861(s)(9)). For coverage under this benefit, the orthosis must be a rigid or semi-rigid device,
which is used for the purpose of supporting a weak or deformed body member or restricting or eliminating motion in
a diseased or injured part of the body. Items that are not sufficiently rigid to be capable of providing the necessary
immobilization or support to the body part for which it is designed do not meet the statutory definition of the braces
benefit. Items that do not meet the definition of a brace are statutorily noncovered, no benefit.

Both “off-the-shelf” (OTS) and custom-fit items are considered prefabricated braces for Medicare coding purposes. 42
CFR §414.402 establishes that correct coding of AFO and KAFO items is dependent upon whether there is a need for
“minimal self-adjustment” during the final fitting at the time of delivery. (See definitions below in CODING
GUIDELINES.) If a custom fit code is billed when minimal self-adjustment was provided at the final delivery, or if an
OTS code is billed when more than minimal self-adjustments were made at the final delivery, the claims will be
denied as incorrect coding.

A static/dynamic ankle-foot orthosis (AFO) (L4396, L4397) and replacement interface (L4392) are denied as
noncovered (no Medicare benefit) when they are used solely for the prevention or treatment of a heel pressure ulcer
because for these indications they are not used to support a weak or deformed body member or to restrict or
eliminate motion in a diseased or injured part of the body (i.e., it does not meet the definition of a brace).

A foot drop splint/recumbent positioning device (L4398) and replacement interface (L4394) are denied as
noncovered (no Medicare benefit) when they are used solely for the prevention or treatment of a pressure ulcer
because for these indications they are not used to support a weak or deformed body member or to restrict or
eliminate motion in a diseased or injured part of the body (i.e., it does not meet the definition of a brace).

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Elastic or other fabric support garments (A4467 (BELT, STRAP, SLEEVE, GARMENT, OR COVERING, ANY TYPE)) with
or without stays or panels do not meet the statutory definition of a brace because they are not rigid or semi-rigid
devices. Code A4467 is denied as noncovered (no Medicare benefit). Refer to the CODING GUIDELINES section below
for additional information.

A foot pressure off-loading/supportive device (A9283) is denied as noncovered (no Medicare benefit), because it does
not support a weak or deformed body member or restrict or eliminate motion in a diseased or injured part of the
body.

An inversion/eversion correction device (A9285) is denied as noncovered (no Medicare benefit), because it does not
act as a brace; that is, it does not support a weak or deformed body member or restrict or eliminate motion in a
diseased or injured part of the body.

Socks (L2840, L2850) used in conjunction with orthoses are denied as noncovered (no Medicare benefit).

Refer to the Orthopedic Footwear policy for information on coverage of shoes and related items which are an integral
part of a brace.

There is no separate payment for computer-aided design/computer-aided manufacturing (CAD/CAM) technology

when it is used to fabricate an orthosis. Reimbursement, of the CAD/CAM technology utilized in the fabrication of an
orthosis, is included in the allowance of the orthosis HCPCS code.

Evaluation of the beneficiary, measurement and/or casting, and fitting/adjustments of the orthosis are included in
the allowance for the orthosis. There is no separate payment for these services.

Payment for ankle-foot orthoses or knee-ankle foot orthoses are included in the payment to a hospital or skilled
nursing facility (SNF) if:

1. The orthosis is provided to a beneficiary prior to an inpatient hospital admission or Part A covered SNF stay;
and,

2. The medical necessity for the orthosis begins during the hospital or SNF stay (e.g., after ankle, foot, or knee
surgery).

A claim should not be submitted to the DME MAC in this situation.

Payment for ankle-foot orthoses or knee-ankle foot orthoses are also included in the payment to a hospital or a Part
A covered SNF stay if:

1. The orthosis is provided to a beneficiary during an inpatient hospital or Part A covered SNF stay prior to the
day of discharge; and,

2. The beneficiary uses the item for medically necessary inpatient treatment or rehabilitation.

A claim must not be submitted to the DME MAC in this situation.

Payment for ankle-foot orthoses or knee-ankle foot orthoses delivered to a beneficiary in a hospital or a Part A
covered SNF stay is eligible for coverage by the DME MAC if:

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 1. The orthosis is medically necessary for a beneficiary after discharge from a hospital or Part A covered SNF
stay; and,

2. The orthosis is provided to the beneficiary within two days prior to discharge to home; and,

3. The orthosis is not needed for inpatient treatment or rehabilitation but is left in the room for the beneficiary to
take home.

REQUIREMENTS FOR SPECIFIC DMEPOS ITEMS PURSUANT TO Final Rule 1713 (84 Fed. Reg Vol 217)

Final Rule 1713 (84 Fed. Reg Vol 217) requires a face-to-face encounter and a Written Order Prior to Delivery
(WOPD) for specified HCPCS codes. CMS and the DME MACs provide a list of the specified codes, which is periodically
updated. The required Face-to-Face Encounter and Written Order Prior to Delivery List is available here.

Claims for the specified items subject to Final Rule 1713 (84 Fed. Reg Vol 217) that do not meet the face-to-face
encounter and WOPD requirements specified in the LCD-related Standard Documentation Requirements Article
(A55426) will be denied as not reasonable and necessary.

If a supplier delivers an item prior to receipt of a WOPD, it will be denied as not reasonable and necessary. If the
WOPD is not obtained prior to delivery, payment will not be made for that item even if a WOPD is subsequently
obtained by the supplier. If a similar item is subsequently provided by an unrelated supplier who has obtained a
WOPD, it will be eligible for coverage.

POLICY SPECIFIC DOCUMENTATION REQUIREMENTS

In addition to policy specific documentation requirements, there are general documentation requirements that are
applicable to all DMEPOS policies. These general requirements are located in the DOCUMENTATION REQUIREMENTS
section of the LCD.

Refer to the LCD-related Standard Documentation Requirements article, located at the bottom of this Policy Article
under the Related Local Coverage Documents section for additional information regarding GENERAL
DOCUMENTATION REQUIREMENTS and the POLICY SPECIFIC DOCUMENTATION REQUIREMENTS discussed below.

General Requirements

The supplier must include on the claim line the diagnosis code(s) for HCPCS codes L4396, L4397, L4392 and L4631.

For a custom-fabricated orthosis, there must be documentation in the supplier's records to support the medical
necessity of that type of device rather than a prefabricated orthosis. This information must be available upon
request.

When providing orthoses suppliers must:

• Provide the product that is specified by the treating practitioner

• Be sure that the treating practitioner's medical record justifies the need for the type of product (i.e.,
prefabricated versus custom fabricated)

• Only bill for the HCPCS code that accurately reflects both the type of orthosis and the appropriate level of

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 fitting

• Have detailed documentation in the supplier's record that justifies the code selected

For prefabricated orthoses (L1902, L1906, L1910, L1930, L1932, L1951, L1971, L2035, L2112, L2114, L2116,
L2132, L2134, L2136, L4350, L4360, L4361, L4370, L4386, L4387, L4396, L4397, L4398), there is no physical
difference between orthoses coded as custom fitted versus those coded as OTS. The differentiating factor for proper
coding (see definitions in CODING GUIDELINES section below) is the need for “minimal self-adjustment” at the time
of fitting by the beneficiary, caretaker for the beneficiary, or supplier. This minimal self-adjustment does not require
the services of a certified orthotist or an individual who has specialized training (as defined in the CODING
GUIDELINES section). Items requiring minimal self-adjustment are coded as OTS orthoses. For example, adjustment
of straps and closures, bending or trimming for final fit or comfort (not all-inclusive) fall into this category.

Items requiring more than minimal self-adjustment by a qualified practitioner (as defined in the CODING
GUIDELINES below) are coded as custom fitted (L1910, L1930, L1932, L1951, L1971, L2035, L2112, L2114, L2116,
L2132, L2134, L2136, L4360, L4386, L4396). Documentation must be sufficiently detailed to include, but is not
limited to, a detailed description of the modifications necessary at the time of fitting the orthosis to the beneficiary.
This information must be available upon request.

For a custom fabricated orthosis (L1900, L1904, L1907, L1920, L1940, L1945, L1950, L1960, L1970, L1980, L1990,
L2000, L2005, L2006, L2010, L2020, L2030, L2034, L2036, L2037, L2038, L2106, L2108, L2126, L2128, L4631),
there must be detailed documentation in the treating practitioner's records to support the medical necessity of the
custom fabricated orthosis rather than a prefabricated orthosis as described in the Coverage Indications, Limitations,
and/or Medical Necessity section of the related LCD. This information will be corroborated by the functional
evaluation in the orthotist's records and the method of custom fabrication should adhere to the DMEPOS Quality
Standards, Appendix C. This information must be available upon request.

MODIFIERS

GA, GZ, KX, LT, and RT MODIFIERS:

Suppliers must add a KX modifier to the AFO/KAFO base and addition codes only if all of the coverage criteria in the
“Coverage Indications, Limitations, and/or Medical Necessity” section in the related LCD have been met and evidence
of such is retained in the supplier’s files and available to the DME MAC upon request.

If all of the criteria in the "Coverage Indications, Limitations, and/or Medical Necessity" section of the related LCD
have not been met, the GA or GZ modifier must be added to the code. When there is an expectation of a medical
necessity denial, suppliers must enter the GA modifier on the claim line if they have obtained a properly executed
Advance Beneficiary Notice (ABN) or the GZ modifier if they have not obtained a valid ABN.

Claim lines billed with codes without a KX, GA or GZ modifier will be rejected as missing information.

The right (RT) and left (LT) modifiers must be used with orthosis base codes, additions, and replacement parts.
Effective for claims with dates of service (DOS) on or after 3/1/2019, when the same code for bilateral items (left
and right) is billed on the same date of service, bill each item on two separate claim lines using the RT and LT
modifiers and 1 unit of service (UOS) on each claim line. Do not use the RTLT modifier on the same claim line and
billed with 2 UOS. Claims billed without modifiers RT and/or LT, or with RTLT on the same claim line and 2 UOS, will
be rejected as incorrect coding.

MISCELLANEOUS

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If the item is custom fabricated and does not have a specific HCPCS code, a complete and clear description of the
item, including what makes this item unique, and a breakdown of charges (material and labor used in fabrication)
should be entered in the narrative field of an electronic claim or on Item 19 of a paper claim. (Refer to the LCD-
related Standard Documentation Requirements article (A55426) for more information regarding billing of items with
HCPCS codes that include miscellaneous, NOC, unlisted, or non-specified in their narrative descriptions.)

A claim for code L4205 must include an explanation of what is being repaired. A claim for code L4210 must include a
description of each item that is billed. This information should be entered in the narrative field of an electronic claim.
(Refer to the REPAIR/REPLACEMENT section for more information regarding billing of L4205 and L4210 HCPCS
codes.)

All codes for orthoses or repairs of orthoses billed with the same date of service must be submitted on the same
claim.

Refer to the Orthopedic Footwear policy for information on documentation requirements for shoes and related items
which are an integral part of a brace.

CODING GUIDELINES

CUSTOM FABRICATED

A custom fabricated item is one that is individually made for a specific patient. No other patient would be able to use
this item. A custom fabricated item is a device which is fabricated based on clinically derived and rectified castings,
tracings, measurements, and/or other images (such as X-rays) of the body part.

The fabrication may involve using calculations, templates, and components. This process requires the use of basic
materials including, but not limited to, plastic, metal, leather, or cloth in the form of uncut or unshaped sheets, bars,
or other basic forms and involves substantial work such as vacuum forming, cutting, bending, molding, sewing,
drilling, and finishing prior to fitting on the patient. Custom-fabricated additions are appropriate only for custom-
fabricated base orthotics and should not be billed with prefabricated base orthotics.

Use of an additive manufacturing technique, CAD/CAM, or a similar manufacturing technique is not the sole
requirement for a product to be designated as custom fabricated.

Molded-to-Patient-Model

A particular type of custom fabricated device in which either:

• An impression (usually by means of a plaster or fiberglass cast) of the specific body part is made directly on
the patient, and this impression is then used to make a positive model of the body part from which the final
product is crafted; or,
• A digital image of the patient’s body part is made using CAD/CAM systems software. This technology includes
specialized probes/digitizers and scanners that create a computerized positive model, and then direct milling
equipment to carve a positive model. The device is then individually fabricated and molded over the positive
model of the patient.

Positive Model of the Patient

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A positive model is an exact replica of the actual body part for which the custom fabricated item is being constructed.
A positive model can be produced by any of these methods:

• Molded-to-patient-model, which is a negative impression taken of the patient’s body member and which is
used to make a positive model rectification.
• CAD/CAM software, which uses digitizers to send surface contour data the practitioner uses to rectify or modify
the model on the computer screen. The data showing the modified shape goes to a commercial milling machine
that carves the rectified model.
• Direct formed model, in which the patient serves as the positive model. The device is constructed over the
patient’s model, and is then fabricated to the patient. The completed custom fabrication is checked and all
necessary adjustments are made.

Additive Manufacturing

Additive manufacturing (such as 3D printing) is an advanced technology that constructs three-dimensional items
modeled and designed from CAD software and/or from digital scanning. Additive manufacturing is an acceptable
custom fabrication technique as long as it adheres to the CMS DMEPOS Quality Standards, Appendix C.

Specialized Training

Specialized training is defined as training that provides knowledge, skills, and experience in the provision of orthotics
in compliance with all applicable Federal and State licensure and regulatory requirements.

PREFABRICATED

A prefabricated orthosis is an item that is manufactured in quantity without a specific beneficiary in mind. A
prefabricated orthosis may be considered an OTS or a custom fitted device that may be trimmed, bent, molded (with
or without heat), or otherwise modified for use by a specific beneficiary. An orthosis that is assembled from
prefabricated components is considered prefabricated. It is inherent in the definition of prefabricated that a particular
item is complete.

Off-the-shelf (OTS) orthotics are:

• Items that are prefabricated.

• They may or may not be supplied as a kit that requires some assembly. Assembly of the item and/or
installation of add-on components and/or the use of some basic materials in preparation of the item does not
change classification from OTS to custom fitted.
• OTS items require minimal self-adjustment for fitting at the time of delivery for appropriate use and do not
require expertise in trimming, bending, and molding, assembling, or customizing to fit an individual.
• This fitting does not require expertise of a certified orthotist or an individual who has specialized training in the
provision of orthoses to fit the item to the individual beneficiary.

The term “minimal self-adjustment” is defined at 42 CFR §414.402 as an adjustment the beneficiary, caregiver for
the beneficiary, or supplier of the device can perform and that does not require the services of a certified orthotist
(that is, an individual who is certified by the American Board for Certification in Orthotics and Prosthetics, Inc., or by
the Board for Orthotist/Prosthetist Certification) or an individual who has specialized training. For example,
adjustment of straps and closures, bending or trimming for final fit or comfort (not all-inclusive) fall into this
category. See “more than minimal self-adjustment” definition below for additional information.

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Custom fitted orthotics are:

• Devices that are prefabricated.

• They may or may not be supplied as a kit that requires some assembly. Assembly of the item and/or
installation of add-on components and/or the use of some basic materials in preparation of the item does not
change classification from OTS to custom fitted.
• Classification as custom fitted requires more than minimal self-adjustment for fitting at the time of delivery in
order to provide an individualized fit, i.e., the item must be trimmed, bent, molded (with or without heat), or
otherwise modified resulting in alterations beyond minimal self-adjustment.
• This fitting at delivery does require expertise of a certified orthotist or an individual who has specialized
training in the provision of the orthosis to fit the item to the individual beneficiary.

In contrast to “minimal self-adjustment,” “more than minimal self-adjustment” is defined as changes made to
achieve an individualized fit during the final fitting at the time of delivery of the item that requires the expertise of a
certified orthotist or an individual who has equivalent specialized training in the provision of orthotics in compliance
with all applicable Federal and State licensure and regulatory requirements. A certified orthotist is defined as an
individual who is certified by the American Board for Certification in Orthotics and Prosthetics, Inc., or by the Board
for Orthotist/Prosthetist Certification.

Correct coding of prefabricated orthoses is dictated by actions that take place at the time of fitting to the beneficiary,
either custom-fitted (requiring expertise) or OTS (requiring minimal self-adjustment).

Corresponding HCPCS Code Sets

For many prefabricated orthoses, corresponding sets of HCPCS codes are available which describe the identical types
of items. The corresponding code sets, when available for identical products, are only differentiated by the nature of
the final fitting performed at the time of delivery. The corresponding HCPCS code types are:

• HCPCS codes which describe “PREFABRICATED, OFF-THE-SHELF.” These HCPCS codes must be used when
minimal self-adjustment is the extent of the fitting performed at delivery.
• HCPCS codes which describe “PREFABRICATED ITEM THAT HAS BEEN TRIMMED, BENT, MOLDED, ASSEMBLED,
OR OTHERWISE CUSTOMIZED TO FIT A SPECIFIC PATIENT BY AN INDIVIDUAL WITH EXPERTISE.” These
HCPCS codes must be used when more than minimal self-adjustment is necessary and performed at delivery.

In the following table, the HCPCS codes located in Column I and Column II within the same row are considered a
corresponding HCPCS code set. These codes represent identical products which are only differentiated by the nature
of the final fitting performed at the time of delivery.

Column I Column II

L4360 L4361

L4386 L4387

L4396 L4397

For some prefabricated orthoses, corresponding sets of HCPCS codes (which describe the identical types of items)

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are not available. HCPCS codes with long descriptions of “PREFABRICATED, INCLUDES FITTING AND ADJUSTMENT”
describe custom fitted items. For these HCPCS codes there are no corresponding OTS codes. When the unique
HCPCS code that most closely describes the product includes “PREFABRICATED, INCLUDES FITTING AND
ADJUSTMENT” in the HCPCS long description, the supplier must:

• Code the product using the unique HCPCS code, if the product was custom fitted at the time of delivery to the
beneficiary; or,
• Code the product using a miscellaneous HCPCS code, if the product was not custom fitted at delivery to the
beneficiary and, instead, was provided as OTS to the beneficiary. The miscellaneous HCPCS code for billing of
AFOs and KAFOs is HCPCS code L2999.

Kits are:

• A collection of components, materials, and parts that require further assembly before delivery of the final
product.
• The elements of a kit may be packaged and complete from a single source or may be an assemblage of
separate components from multiple sources by the supplier.

ELASTIC AND SIMILAR STRETCHABLE MATERIALS

For items where the HCPCS code specifies “elastic” or other similar terminology for stretchable material, use the code
that is most applicable to the item. A NOC (Not Otherwise Classified) or miscellaneous HCPCS code must not be used
instead of the specific code. Refer to the long code narrative and any relevant coding guideline for the criteria
applicable for each HCPCS code.

For items where the HCPCS code does not specify elastic or other similar terminology for stretchable material, the
following guidelines apply:

• Items that are primarily constructed of elastic or other stretchable materials (e.g. support items made of
material such as neoprene or spandex (elastane, Lycra®) (not all-inclusive)) must be coded as A4467 (BELT,
STRAP, SLEEVE, GARMENT, OR COVERING, ANY TYPE).
• Items that are primarily constructed of elastic or other stretchable materials (e.g. support items made of
material such as neoprene or spandex (elastane, Lycra®]) (not all-inclusive)) that contain stays and/or panels
must be coded as A4467 (BELT, STRAP, SLEEVE, GARMENT, OR COVERING, ANY TYPE).
• Items that are primarily constructed of inelastic material (e.g., canvas, cotton or nylon (not all-inclusive)) that
are incapable of providing the necessary immobilization or support to the body part for which it is designed
must be coded using A4467 (BELT, STRAP, SLEEVE, GARMENT, OR COVERING, ANY TYPE).
• Items that are primarily of constructed inelastic material (e.g., canvas, cotton or nylon (not all-inclusive)) that
are incapable of providing the necessary immobilization or support to the body part for which it is designed and
that have stays and/or panels capable of providing the required immobilization or support to the body part for
which it is designed, must be coded using A4467 (BELT, STRAP, SLEEVE, GARMENT, OR COVERING, ANY
TYPE).
• Items that are primarily constructed of inelastic material (e.g., canvas, cotton or nylon (not all-inclusive))
capable of providing the necessary immobilization or support to the body part for which it is designed must be
coded using the applicable specific HCPCS code for the type of product. A NOC (Not Otherwise Classified) or
miscellaneous HCPCS code must not be used instead of the specific code. Refer to the long code narrative and
any relevant coding guideline for the criteria applicable for each HCPCS code.
• Items that are primarily of constructed inelastic material (e.g., canvas, cotton or nylon (not all-inclusive))
capable of providing the necessary immobilization or support to the body part for which it is designed and that

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 have stays and/or panels capable of providing the required immobilization or support to the body part for
which it is designed, must be coded using the applicable specific HCPCS code for the type of product. A NOC
(Not Otherwise Classified) or miscellaneous HCPCS code must not be used instead of the specific code. Refer to
the long code narrative and relevant coding guideline for the criteria applicable for each HCPCS code.
• Items that are not capable of providing the necessary immobilization or support to the body part for which it is
designed (regardless of materials) must be coded using A9270 (NONCOVERED ITEM OR SERVICE).

ANKLE-FOOT-ORTHOSES

Ankle-foot orthoses described by codes L1900, L1910, L1920, L1930, L1932, L1940, L1945, L1950, L1951, L1960,
L1970, L1971, L1980, L1990, extend well above the ankle (usually to near the top of the calf) and are fastened
around the lower leg above the ankle. These features distinguish them from foot orthotics which are shoe inserts that
do not extend above the ankle and ankle gauntlets described by codes L1902, L1904, L1906, L1907.

L1900 (ANKLE FOOT ORTHOSIS, SPRING WIRE, DORSIFLEXION ASSIST CALF BAND, CUSTOM FABRICATED)
describes a custom fabricated AFO designed to control inversion, eversion, dorsiflexion, and plantarflexion motions of
the ankle foot complex. Primary construction is of two springwire uprights, which are joined to a rigid calf band/cuff,
and a component for attaching the orthosis to the sole of an orthopedic shoe. The springwire is contoured into a
coiled spring below the ankle and above the shoe sole. The height of the rigid calf band/cuff terminates well-above
the ankle (usually near the top of the calf) and the band/cuff is fastened around the lower leg above the ankle. The
coiled springwire applies a spring force to resist plantarflexion motion and provide dorsiflexion assist. Included in the
code are closure components, and attaching spring wire to the footwear. This AFO is custom fabricated per the
DMEPOS quality standards, Appendix C.

L1902 (ANKLE ORTHOSIS, ANKLE GAUNTLET OR SIMILAR, WITH OR WITHOUT JOINTS, PREFABRICATED, OFF-THE-
SHELF) describes a prefabricated ankle orthosis (AO) designed to provide compression and resist motion of the ankle
foot complex. Primary construction is a sleeve type device (gauntlet) with or without joints. The gauntlet encloses
the foot and ankle from the longitudinal arch to at least just above the malleoli. Gauntlet closure may be straps,
hook and loop, laces or equal. The orthosis may or may not include joints or hinges for additional support. There are
no additional HCPCS codes for this type of prefabricated ankle orthosis.

L1904 (ANKLE ORTHOSIS, ANKLE GAUNTLET OR SIMILAR, WITH OR WITHOUT JOINTS, CUSTOM FABRICATED)
describes a custom fabricated AO designed to provide compression and resist motion of the ankle foot complex.
Primary construction is a sleeve type device (gauntlet) with or without joints. The gauntlet encloses the foot and
ankle from the longitudinal arch to at least just above the malleoli. Gauntlet closure may be straps, hook and loop,
laces or equal. The orthosis may or may not include joints or hinges for additional support. This AO is custom
fabricated per the DMEPOS quality standards, Appendix C.

L1906 (ANKLE FOOT ORTHOSIS, MULTILIGAMENTOUS, ANKLE SUPPORT, PREFABRICATED, OFF-THE-SHELF)

describes a prefabricated AFO which provides multi-directional support to the ankle ligaments while allowing free
dorsiflexion and plantarflexion motion. Primary construction contains a rigid footplate with integral ankle joints and
uprights extending above and below the ankle joints. Proximal uprights provide surface area contact for stabilization
of the footplate and ankle joints. Additional support is from wraparound straps. Included in the code are closures
from lacing, webbing, hook and loop, or equal, and additional support strapping. There are no additional HCPCS
codes for this type of prefabricated ankle foot orthosis.

L1907 (ANKLE ORTHOSIS, SUPRAMALLEOLAR WITH STRAPS, WITH OR WITHOUT INTERFACE/PADS, CUSTOM
FABRICATED) describes a custom fabricated AO designed to control motion of the ankle and mid-foot. Primary
construction is of molded plastic designed to control inversion and eversion, and horizontal rotation motions while

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allowing dorsiflexion and plantarflexion motion of the ankle joint. Included in the code are closure components, soft
interface and padding. Trim lines extend from tips of toes to just above the malleoli. This AO is custom fabricated per
the DMEPOS quality standards, Appendix C.

L1910 (ANKLE FOOT ORTHOSIS, POSTERIOR, SINGLE BAR, CLASP ATTACHMENT TO SHOE COUNTER,
PREFABRICATED, INCLUDES FITTING AND ADJUSTMENT) describes a prefabricated AFO designed to control
dorsiflexion and plantarflexion motions of the ankle foot complex. Primary construction is a single flexible upright
utilizing a removable clasp-type component attached to the heel portion of a shoe and a rigid calf band/cuff. Height
of the rigid calf band/cuff terminates well above the ankle (usually near the top of the calf) and is fastened around
the lower leg above the ankle. Included in the code are closure and clasp components. There are no additional
HCPCS codes for this type of prefabricated ankle foot orthosis.

L1920 (ANKLE FOOT ORTHOSIS, SINGLE UPRIGHT WITH STATIC OR ADJUSTABLE STOP (PHELPS OR PERLSTEIN
TYPE), CUSTOM FABRICATED) describes a custom fabricated AFO designed to control only the plantarflexion motion
of the ankle foot complex. Primary construction is a single metal upright which has a pivoting attachment into a sole
component attached to an orthopedic shoe. The single rigid upright is joined to a rigid calf band/cuff which
terminates well-above the ankle (usually near the top of the calf) and is fastened around the lower leg above the
ankle. The pivoting attachment has an integrated component(s) to stop plantarflexion ankle motion while always
allowing free dorsiflexion motion. Included in the code are components for closures and attaching the footwear. This
AFO is custom fabricated per the DMEPOS quality standards, Appendix C.

L1930 (ANKLE FOOT ORTHOSIS, PLASTIC OR OTHER MATERIAL, PREFABRICATED, INCLUDES FITTING AND
ADJUSTMENT) describes a prefabricated AFO designed to control inversion, eversion, dorsiflexion, and plantarflexion
motions of the ankle foot complex. Primary construction is a rigid calf cuff and rigid foot plate section joined by a
flexible posterior strut. The foot plate must extend to the metatarsal heads and may extend as far as the toe tips.
Calf cuff height terminates well-above the ankle (usually near the top of the calf) and is fastened around the lower
leg above the ankle and footplate may extend to toe tip. This AFO is constructed from plastic or other materials.
Included in the code are closure components.

L1932 (AFO, RIGID ANTERIOR TIBIAL SECTION, TOTAL CARBON FIBER OR EQUAL MATERIAL, PREFABRICATED,
INCLUDES FITTING AND ADJUSTMENT) describes a prefabricated AFO designed to control the dorsiflexion and
plantarflexion, and inversion and eversion, motions of the ankle foot complex. Primary construction includes full
length foot plate, rigid front shin shell that extends from lower shin region to near tibial tubercle. Rigid strut connects
foot plate to shin shell. This AFO is constructed of carbon fiber or equal. Included in the code are closure components
and soft interface. There are no additional HCPCS codes for this type of prefabricated ankle foot orthosis.

L1940 (ANKLE FOOT ORTHOSIS, PLASTIC OR OTHER MATERIAL, CUSTOM FABRICATED) describes a custom
fabricated AFO designed to control inversion, eversion, dorsiflexion, and plantarflexion motions of the ankle foot
complex. Primary construction includes rigid foot plate, strut or equal component, which joins footplate to a calf cuff.
Calf cuff height terminates well above the ankle (usually to near the top of the calf) and are fastened around the
lower leg above the ankle. This AFO can be constructed from flexible and strong thermosetting materials,
thermoplastics, or composite type materials. Included in the code are closure components. This AFO is custom
fabricated per the DMEPOS quality standards, Appendix C.

L1945 (ANKLE-FOOT ORTHOSIS (AFO), PLASTIC, RIGID ANTERIOR TIBIAL SECTION (FLOOR REACTION), CUSTOM
FABRICATED) describes a custom fabricated AFO designed to control inversion, eversion, dorsiflexion, plantarflexion,
and horizontal rotation motions of the ankle foot complex. Primary construction is a plastic full-length rigid foot plate,
rigid shell with Anterior calf cuff typically extending from mid-shin region to tibial tubercle. Rigid strut connects foot
plate to shin shell. Shell cutouts are created to aid donning of the AFO. This AFO is constructed of plastic materials.

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Included in the code are closure components. This AFO is custom fabricated per the DMEPOS quality standards,
Appendix C.

L1950 (ANKLE FOOT ORTHOSIS, SPIRAL, (INSTITUTE OF REHABILITATIVE MEDICINE TYPE), PLASTIC, CUSTOM
FABRICATED) describes a custom fabricated AFO designed to control inversion, eversion, dorsiflexion, plantarflexion,
and horizontal rotation motions of the ankle foot complex. Primary construction includes, at minimum, a 90-degree
spiral-shaped strut joining the rigid footplate to the rigid calf cuff. Foot plate must extend to the metatarsal heads
and may extend as far as the toe tips. Calf cuff height terminates well above the ankle (usually to near the top of the
calf) and are fastened around the lower leg above the ankle. This AFO can be constructed from flexible and strong
thermosetting materials, thermoplastics, or composite type materials. Included in the code are closure components.
This AFO is custom fabricated per the DMEPOS quality standards, Appendix C.

L1951 (ANKLE FOOT ORTHOSIS, SPIRAL, (INSTITUTE OF REHABILITATIVE MEDICINE TYPE), PLASTIC OR OTHER
MATERIAL, PREFABRICATED, INCLUDES FITTING AND ADJUSTMENT) describes a prefabricated AFO designed to
control dorsiflexion and plantarflexion motions of the ankle foot complex. Primary construction includes, at minimum,
a 90-degree spiral-shaped strut linking the footplate to the rigid calf cuff. Foot plate must extend to the metatarsal
heads and may extend as far as the toe tips. Calf cuff height terminates well above the ankle (usually to near the top
of the calf) and are fastened around the lower leg above the ankle. The AFO can be constructed from flexible and
strong thermosetting materials, thermoplastics, or composite type materials. Included in the code are closure
components. There are no additional HCPCS codes for this type of prefabricated ankle foot orthosis.

L1960 (ANKLE FOOT ORTHOSIS, POSTERIOR SOLID ANKLE, PLASTIC, CUSTOM FABRICATED) describes an AFO
which provides ankle control for beneficiaries with musculoskeletal or neuromuscular dysfunction. The AFO is
designed to provide rigid immobilization of the ankle-foot complex in the sagittal, coronal, and transverse planes.
The custom fabricated solid ankle AFO can be constructed from thermosetting materials, thermoplastics, or
composite type materials. This AFO is custom fabricated per the DMEPOS quality standards, Appendix C.

L1970 (ANKLE FOOT ORTHOSIS, PLASTIC WITH ANKLE JOINT, CUSTOM FABRICATED) describes a custom fabricated
AFO designed to control inversion, eversion, dorsiflexion, plantarflexion, and horizontal rotation motions of the ankle
foot complex. Primary construction is a rigid shell-like or equal structure containing a hinge or joint mechanism.
Structure contacts calf, lower leg, and foot to provide control. Foot plate must extend to the metatarsal heads and
may extend as far as the toe tips. Calf cuff height terminates well above the ankle (usually to near the top of the
calf) and are fastened around the lower leg above the ankle. This AFO can be constructed from thermosetting
materials, thermoplastics, or composite type materials. Included in the code are closure components. This AFO is
custom fabricated per the DMEPOS quality standards, Appendix C.

L1971 (ANKLE FOOT ORTHOSIS, PLASTIC OR OTHER MATERIAL WITH ANKLE JOINT, PREFABRICATED, INCLUDES
FITTING AND ADJUSTMENT) describes a prefabricated AFO designed to control inversion, eversion, dorsiflexion,
plantarflexion, and horizontal rotation motions of the ankle foot complex. Primary construction is a rigid shell-like or
equal structure containing a hinge or joint mechanism. Structure contacts calf, lower leg, and foot to provide control.
Foot plate must extend to the metatarsal heads and may extend as far as the toe tips. Calf cuff height terminates
well above the ankle. Included in the code are closure components.

L1980 (ANKLE FOOT ORTHOSIS, SINGLE UPRIGHT FREE PLANTAR DORSIFLEXION, SOLID STIRRUP, CALF
BAND/CUFF (SINGLE BAR 'BK' ORTHOSIS), CUSTOM FABRICATED) describes a custom fabricated AFO designed to
control inversion and eversion motions of the ankle foot complex. Primary construction is a single metal upright
(medial or lateral) joined to a rigid calf band, free motion ankle joint, and stirrup component attached to an
orthopedic shoe. Height of calf cuff/band terminates well above the ankle (usually to near the top of the calf) and is
fastened around the lower leg above the ankle. Included in the code are components for closures and attaching the

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footwear. This AFO is custom fabricated per the DMEPOS quality standards, Appendix C.

L1990 (ANKLE FOOT ORTHOSIS, DOUBLE UPRIGHT FREE PLANTAR DORSIFLEXION, SOLID STIRRUP, CALF
BAND/CUFF (DOUBLE BAR 'BK' ORTHOSIS), CUSTOM FABRICATED) describes a custom fabricated AFO designed to
control inversion and eversion motions of the ankle foot complex. Primary construction are two metal uprights
(medial and lateral) joined to a rigid calf band, free motion ankle joints, and stirrup component attached to an
orthopedic shoe. Height of calf cuff/band terminates well above the ankle (usually to near the top of the calf) and is
fastened around the lower leg above the ankle. Included in the code are components for closures and attaching the
footwear. This AFO is custom fabricated per the DMEPOS quality standards, Appendix C.

Code L4631 describes a Charcot’s restraint orthotic walker (CROW) orthosis. Code L4631 is a custom fabricated
ankle-foot orthosis which has all of the following characteristics:

1. Designed to maintain the foot at a fixed position of 0° (i.e., perpendicular to the lower leg); and,

2. Allows for varus or valgus deformity correction; and,

3. Contains a rocker bottom sole with a custom arch support; and,

4. Incorporates a rigid anterior tibial shell; and,

5. Used by a beneficiary who is ambulatory; and,

6. Has a soft interface

7. Totally encapsulated.

Code L4631 includes all additions including straps and closures. No additional codes may be billed with code L4631.

KNEE-ANKLE-FOOT ORTHOSES

L2005 (KNEE ANKLE FOOT ORTHOSIS, ANY MATERIAL, SINGLE OR DOUBLE UPRIGHT, STANCE CONTROL,
AUTOMATIC LOCK AND SWING PHASE RELEASE, ANY TYPE ACTIVATION, INCLUDES ANKLE JOINT, ANY TYPE,
CUSTOM FABRICATED) describes a custom fabricated, single or double upright KAFO with an automatic lock and
swing phase release knee joint. Automatic knee lock is activated by any method such as mechanical or electrical. The
custom fabricated KAFO can be constructed from thermosetting materials, thermoplastics, or composite type
materials. It includes any type ankle joint and closure components. There are no additional add-on codes for L2005.
This KAFO is custom fabricated per the DMEPOS Quality Standards, Appendix C.

L2006 (KNEE ANKLE FOOT DEVICE, ANY MATERIAL, SINGLE OR DOUBLE UPRIGHT, SWING AND STANCE PHASE
MICROPROCESSOR CONTROL WITH ADJUSTABILITY, INCLUDES ALL COMPONENTS (E.G., SENSORS, BATTERIES,
CHARGER), ANY TYPE ACTIVATION, WITH OR WITHOUT ANKLE JOINT(S), CUSTOM FABRICATED) describes a custom
fabricated, single or double upright KAFO with an adjustable microprocessor control feature which provides
resistance to stance and swing phase knee joint motion. The custom fabricated KAFO can be constructed from
thermosetting materials, thermoplastics, or composite type materials. There are no additional add-on codes for this
KAFO. This KAFO is custom fabricated per the DMEPOS Quality Standards, Appendix C.

L2034 (KNEE ANKLE FOOT ORTHOSIS, FULL PLASTIC, SINGLE UPRIGHT, WITH OR WITHOUT FREE MOTION KNEE,
MEDIAL LATERAL ROTATION CONTROL, WITH OR WITHOUT FREE MOTION ANKLE, CUSTOM FABRICATED) describes
a custom fabricated, single upright KAFO designed to control (1) knee flexion, extension, and rotation motions (2)
ankle inversion, eversion, dorsiflexion, plantarflexion, and rotation motions of the ankle foot complex. Primary

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construction is a rigid shell-like or equal structure which can be; (1) with or without free range of motion knee hinge
or joint mechanism; (2) with or without free range of motion ankle hinge(s). Through a series of straps/supports that
cross over and around the knee joint, rotational control and varus or valgus force is exerted on the knee joint.
Structure contacts thigh, calf, lower leg, and foot to provide control. Foot plate must extend to the metatarsal heads.
The custom fabricated KAFO can be constructed from thermosetting materials, thermoplastics, or composite type
materials. Included in the code are closure components. The predicate product is the Generation II KAFO with hinged
ankle manufactured by Generation II USA, Inc. This KAFO is custom fabricated per the DMEPOS Quality Standards,
Appendix C.

L2036 (KNEE ANKLE FOOT ORTHOSIS, FULL PLASTIC, DOUBLE UPRIGHT, WITH OR WITHOUT FREE MOTION KNEE,
WITH OR WITHOUT FREE MOTION ANKLE, CUSTOM FABRICATED) describes a custom fabricated, double upright
KAFO designed to control (1) knee flexion, extension, rotation motions (2) ankle inversion, eversion, dorsiflexion,
plantarflexion, and rotation motions of the ankle foot complex. Primary construction is a rigid shell-like or equal
structure which can be with or without free range of motion hinge or joint mechanisms at the knee and/or ankle.
Structure contacts thigh, calf, lower leg, and foot to provide control. Foot plate must extend to the metatarsal heads.
The custom fabricated KAFO can be constructed from thermosetting materials, thermoplastics, or composite type
materials. Included in the code are closure components. This KAFO is custom fabricated per the DMEPOS Quality
Standards, Appendix C.

LOWER EXTREMITY ADDITIONS

Custom-fabricated additions are appropriate only for custom-fabricated base orthotics and should not be billed with
prefabricated base orthotics unless a product has been previously assigned an addition code per PDAC/CMS prior to
1/1/2023. Correct coding with use of addition codes should not include, or partially include, features or functions
described by other codes billed for a specific device.

L2200 (ADDITION TO LOWER EXTREMITY, LIMITED ANKLE MOTION, EACH JOINT) describes an ankle joint product
which can control dorsiflexion and/or plantarflexion of the ankle joint. The range of motion is set during fabrication.
Joints can be deployed as a pair (two UOS) or singly (one UOS) with appropriate custom fabricated AFO or KAFO.
Product will be distinctly identifiable from other components of the orthosis.

L2210 (ADDITION TO LOWER EXTREMITY, DORSIFLEXION ASSIST (PLANTAR FLEXION RESIST), EACH JOINT)
describes an ankle joint product which can control plantarflexion of the ankle joint. The range of motion is adjustable
post-delivery of the orthosis. Initial setting is set by the supplier during fabrication. Joints can be deployed as a pair
(two UOS) or singly (one UOS) with appropriate custom fabricated AFO or KAFO. Product will be distinctly identifiable
from other components of the orthosis.

L2220 (ADDITION TO LOWER EXTREMITY, DORSIFLEXION AND PLANTAR FLEXION ASSIST/RESIST, EACH JOINT)
describes an ankle joint product which can control dorsiflexion and/or plantarflexion of the ankle joint. The range of
motion is adjustable post-delivery of the orthosis. Initial setting is set by the supplier during fabrication. Joints can
be deployed as a pair (two UOS) or singly (one UOS) with appropriate custom fabricated AFO or KAFO. Product will
be distinctly identifiable from other components of the orthosis.

L2280 (ADDITION TO LOWER EXTREMITY, MOLDED INNER BOOT) describes a custom molded device which encircles
the ankle and to at least the mid-foot to provide multi-directional support to the ankle foot complex with
compression from semi-rigid or rigid material(s). Inner boot is fully circumferential with closure components included
such as lacing/eyelets or hook/loop. Lacer material and construction must conform to DMEPOS Quality Standards,
Appendix C.

Created on 02/13/2025. Page 15 of 29

L2330 (ADDITION TO LOWER EXTREMITY, LACER MOLDED TO PATIENT MODEL, FOR CUSTOM FABRICATED
ORTHOSIS ONLY) describes an upgrade to the cuff (including closures) to cover the rigid structures of the orthosis.
Custom fabrication would capture shapes and contours of the anatomy to improve function of the included
cuff/closure component. Lacer is fully circumferential with closure components included such as lacing/eyelets or
hook/loop. Lacer material and construction must conform to DMEPOS Quality Standards, Appendix C.

L2340 (ADDITION TO LOWER EXTREMITY, PRE-TIBIAL SHELL, MOLDED TO PATIENT MODEL) is a pre-tibial shell,
custom fabricated, that provides a rigid overlapping interlocking anterior tibial control between the tibial tuberosity to
a point no greater than 3 inches proximal to the medial malleolus. The pre-tibial shell can be constructed from
thermosetting materials, thermoplastics, or composite type materials.

Code L2755 (ADDITION TO LOWER EXTREMITY ORTHOSIS, HIGH STRENGTH, LIGHTWEIGHT MATERIAL, ALL HYBRID
LAMINATION/PREPREG COMPOSITE, PER SEGMENT, FOR CUSTOM FABRICATED ORTHOSIS ONLY) describes an
addition to a lower extremity orthosis composed of high strength and/or lightweight material such as Kevlar®,
carbon fiber or other laminated or impregnated composite material.

L2820 (ADDITION TO LOWER EXTREMITY ORTHOSIS, SOFT INTERFACE FOR MOLDED PLASTIC, BELOW KNEE
SECTION) describes a moldable and compliant material which has been fabricated as an integral part of a custom
fabricated orthosis. The interface is designed to allow cushioning and contouring over pressure-sensitive areas of the
limb in greater capacity than what may be included in the base orthosis that is constructed from thermosetting
materials, thermoplastics, or composite type materials. The soft interface material and construction must conform to
DMEPOS Quality Standards, Appendix C.

POSITIONING DEVICES

A non-ambulatory ankle-foot orthosis may be either an ankle contracture splint, night splint or a foot drop splint.

A static or dynamic positioning ankle-foot orthosis (L4396, L4397) is a prefabricated ankle-foot orthosis which has all
of the following characteristics:

1. Designed to accommodate either plantar fasciitis or an ankle with a plantar flexion contracture up to 45°; and,

2. Applies a dorsiflexion force to the ankle; and,

3. Used by a beneficiary who is minimally ambulatory, or non-ambulatory; and,

4. Has a soft interface.

A foot drop splint/recumbent positioning device (L4398) is a prefabricated ankle-foot orthosis which has all of the
following characteristics:

1. Designed to maintain the foot at a fixed position of 0° (i.e., perpendicular to the lower leg); and,

2. Not designed to accommodate an ankle with a plantar flexion contracture; and,

3. Used by a beneficiary who is non-ambulatory; and,

4. Has a soft interface.

SHOE INSERTS

Created on 02/13/2025. Page 16 of 29

Foot orthoses are shoe inserts that do not extend above the ankle. Shoes, inserts, and shoe modifications that are
integral components of a leg brace are referred to as orthopedic footwear (ORF). These shoes, inserts, and shoe
modifications are only covered if they are an integral part of a covered leg brace that is described by HCPCS code
L1900, L1920, L1980, L1990, L2000, L2005, L2010, L2020, L2030, L2050, L2060, L2080, or L2090. In addition to
being an integral component of the covered leg brace, these products must also be medically necessary for the
proper functioning of the leg brace. When billing for ORF, the leg brace and ORF must be billed by the same supplier
(refer to the Orthopedic Footwear policy for more information).

Multiple density foot orthotics that are provisioned in the treatment of a beneficiary’s diabetes-related condition(s),
must not be billed using L-codes but rather must be billed using A-codes. The A-codes for billing of such foot
orthotics are A5512, A5513, and A5514 (code A5514 effective for DOS on or after 01/01/2019) (refer to the
Therapeutic Shoes for Persons with Diabetes policy for more information).

CONCENTRIC TORSION JOINTS

All claims for devices that contain a concentric adjustable torsion style mechanism in the knee joint for any condition
other than an assistive function to joint extension motion must be coded as durable medical equipment using code
E1810 (DYNAMIC ADJUSTABLE KNEE EXTENSION AND FLEXION DEVICE, INCLUDES SOFT INTERFACE MATERIAL),
E1813 (DYNAMIC ADJUSTABLE KNEE EXTENSION ONLY DEVICE, INCLUDES SOFT INTERFACE MATERIAL), or E1814
(DYNAMIC ADJUSTABLE KNEE FLEXION ONLY DEVICE, INCLUDES SOFT INTERFACE MATERIAL). If a concentric
adjustable torsion style mechanism in the knee joint is used solely to provide an assistive function for joint
extension, it must be coded as L2999 (See Coverage Indications, Limitations, and/or Medical Necessity section of the
related LCD).

All claims for devices that contain a concentric adjustable torsion style mechanism in the ankle joint for any condition
other than an assistive function to joint plantar- or dorsiflexion motion must be coded as durable medical equipment
using code E1815 (DYNAMIC ADJUSTABLE ANKLE EXTENSION AND FLEXION DEVICE, INCLUDES SOFT INTERFACE
MATERIAL), E1822 (DYNAMIC ADJUSTABLE ANKLE EXTENSION ONLY DEVICE, INCLUDES SOFT INTERFACE
MATERIAL), or E1823 (DYNAMIC ADJUSTABLE ANKLE FLEXION ONLY DEVICE, INCLUDES SOFT INTERFACE
MATERIAL). If a concentric adjustable torsion style mechanism in the ankle joint is used solely to provide an assistive
function for joint plantar or dorsiflexion, it must be coded as L2999 (See Coverage Indications, Limitations, and/or
Medical Necessity section of the related LCD).

Claims for devices that contain a concentric adjustable torsion style mechanism in the knee or ankle joint and that
are being used to treat any condition other than an assistive function to joint extension motion are not covered under
the braces benefit and will be denied as incorrect coding when billed using code L2999 (See Coverage Indications,
Limitations, and/or Medical Necessity section of the related LCD).

WALKING BOOTS

Prefabricated walking boots are coded using codes L4360, L4361, L4386 or L4387. These codes describe complete
products. Claims for add-on codes used with walking boots coded L4360, L4361, L4386 or L4387 will be denied as
unbundling.

Certain products may have both covered and non-covered uses, as defined by the braces benefit category, and must
be coded based on the beneficiary’s condition. For example, when used as a brace for the treatment of an orthopedic
condition, walking boots are coded L4360, L4361, L4386, L4387 and L4631. However, walking boots must be coded
A9283 when used solely for the prevention or treatment of a lower extremity ulcer or pressure reduction.

OTHER DEVICES

Created on 02/13/2025. Page 17 of 29

Code A9283 (FOOT PRESSURE OFF LOADING/SUPPORTIVE DEVICE, ANY TYPE, EACH) is used for an item that is
designed primarily to reduce pressure on the sole or heel of the foot. It may be a shoe-like item, an item that is used
inside a shoe and may or may not extend outside the shoe, or an item that is attached to a shoe. It may be
prefabricated or custom fabricated. Code A9283 does not include items that meet the definition of a therapeutic shoe
for diabetes (A5500, A5501).

When using code A9283, there is no separate billing using addition codes. Replacement liners for devices billed with
A9283 must be billed with code A9270 (NON-COVERED ITEM OR SERVICE).

Code A9285 (INVERSION/EVERSION CORRECTION DEVICE) is designed to provide off-loading pressure to the knee
for the treatment of knee osteoarthritis. The device is applied at the foot and extends across the ankle to apply
pressure to the side of the leg below the knee. It does not provide any support at the ankle.

REPAIR/REPLACEMENT

Code L4205 (REPAIR OF ORTHOTIC DEVICE, LABOR COMPONENT, PER 15 MINUTES) may only be billed for time
involved with the actual repair of an orthosis or for medically necessary adjustments made more than 90 days after
delivery. Code L4205 must not be used to bill for time involved with other professional services including, but not
limited to:

• Evaluating the beneficiary

• Taking measurements, making a cast, making a model, use of CAD/CAM
• Making modifications to a prefabricated item to fit it to the individual beneficiary
• Follow-up visits
• Making adjustments at the time of or within 90 days after delivery

Suppliers must distinguish between repair and replacement of an orthosis. When an orthotic is replaced, there is no
separate billing for the above services because reimbursement for these services is included in the allowance for the
replacement item.

Repairs to a covered orthosis due to wear or to accidental damage are covered when they are necessary to make the
orthosis functional. The reason for the repair must be documented in the supplier's record. If the expense for repairs
exceeds the estimated expense of providing another entire orthosis, no payment will be made for the amount in
excess.

The allowance for the labor involved in replacing an orthotic component that is coded with a specific L-code is
included in the allowance for that component. The allowance for the labor involved in replacing an orthotic
component that is coded with the miscellaneous code L4210 is separately payable in addition to the allowance for
that component.

Addition codes L4002, L4010, L4020, L4030, L4040, L4045, L4050, L4055, L4060, L4070, L4080, L4090, L4100,
L4110, L4130, and L4392 are for billing of replacement components and are not payable at initial issue of a base
orthosis. When claims for code(s) L4002, L4010, L4020, L4030, L4040, L4045, L4050, L4055, L4060, L4070, L4080,
L4090, L4100, L4110, L4130, and L4392 are billed at the time of initial issue of a base orthosis, the addition code(s)
will be rejected as incorrect coding.

Suppliers should contact the Pricing, Data Analysis, and Coding (PDAC) contractor for guidance on the correct coding
of these items.

HCPCS codes L4050 and L4055 do not describe replacement soft interfaces used with contracture orthoses.

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Some replacement items have unique Healthcare Common Procedure Coding System (HCPCS) codes. Replacement
components that do not have a unique HCPCS code must be billed with a "not otherwise specified" code - L2999.
Items that have unique codes must not be billed using a NOC code.

CODING VERIFICATION REVIEW

The only products which may be billed using the following list of HCPCS codes are those for which a written coding
verification review (CVR) has been made by the PDAC contractor and subsequently published on the Product
Classification List (PCL). Information concerning the documentation that must be submitted to the PDAC for a CVR
can be found on the PDAC web site or by contacting the PDAC. A PCL with products which have received a coding
verification can be found on the PDAC web site. The effective date of the CVR is included for each code.

Effective for claims with dates of service on or after April 1, 2012:

L1906

Effective for claims with dates of service on or after January 1, 2020:

L2006

Effective for claims with dates of service on or after December 1, 2024:

L1951

If a product is billed to Medicare using a HCPCS code that requires written CVR, but the product is not on the PCL for
that particular HCPCS code, then the claim line will be denied as incorrect coding.

Coding Information

CPT/HCPCS Codes

N/A

ICD-10-CM Codes that Support Medical Necessity

Group 1 Paragraph:

The presence of an ICD-10 code listed in this section is not sufficient by itself to assure coverage. Refer to the LCD
section on “Coverage Indications, Limitations, and/or Medical Necessity” for other coverage criteria and
payment information.

For HCPCS codes L4392, L4396 and L4397:

Group 1 Codes: (5 Codes)

CODE DESCRIPTION

M24.571 Contracture, right ankle

M24.572 Contracture, left ankle

M24.574 Contracture, right foot

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CODE DESCRIPTION

M24.575 Contracture, left foot

M72.2 Plantar fascial fibromatosis

Group 2 Paragraph:

For HCPCS code L4631:

Group 2 Codes: (7 Codes)

CODE DESCRIPTION

A52.16 Charcot's arthropathy (tabetic)

E08.610 Diabetes mellitus due to underlying condition with diabetic neuropathic arthropathy

E09.610 Drug or chemical induced diabetes mellitus with diabetic neuropathic arthropathy

E10.610 Type 1 diabetes mellitus with diabetic neuropathic arthropathy

E11.610 Type 2 diabetes mellitus with diabetic neuropathic arthropathy

M14.671 Charcot's joint, right ankle and foot

M14.672 Charcot's joint, left ankle and foot

ICD-10-CM Codes that DO NOT Support Medical Necessity

Group 1 Paragraph:

For the specific HCPCS codes indicated above, all ICD-10 codes that are not specified in the preceding section. For
all other HCPCS codes, diagnoses are not specified.

Group 1 Codes:

N/A

ICD-10-PCS Codes

N/A

Additional ICD-10 Information

N/A

Bill Type Codes

Contractors may specify Bill Types to help providers identify those Bill Types typically used to report this service.
Absence of a Bill Type does not guarantee that the article does not apply to that Bill Type. Complete absence of all
Bill Types indicates that coverage is not influenced by Bill Type and the article should be assumed to apply equally
to all claims.

Created on 02/13/2025. Page 20 of 29

N/A

Revenue Codes

Contractors may specify Revenue Codes to help providers identify those Revenue Codes typically used to report
this service. In most instances Revenue Codes are purely advisory. Unless specified in the article, services
reported under other Revenue Codes are equally subject to this coverage determination. Complete absence of all
Revenue Codes indicates that coverage is not influenced by Revenue Code and the article should be assumed to
apply equally to all Revenue Codes.

N/A

Revision History Information

REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

01/01/2025 R18
Revision Effective Date: 01/01/2025
CODING GUIDELINES:
Revised: Long descriptions for HCPCS codes E1810 and E1815
Added: HCPCS codes E1813 and E1814 to the HCPCS codes noted as codes for durable
medical equipment that are used when coding claims for devices that contain a
concentric adjustable torsion style mechanism in the knee joint for any condition other
than an assistive function to joint extension motion
Added: HCPCS codes E1822 and E1823 to the HCPCS codes noted as codes for durable
medical equipment that are used when coding claims for devices that contain a
concentric adjustable torsion style mechanism in the ankle joint for any condition other
than an assistive function to joint plantar- or dorsiflexion motion

01/16/2025: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

01/23/2024 R17
Revision Effective Date: 01/23/2024
CODING VERIFICATION REVIEW:
Added: Coding verification review information for HCPCS code L1951, effective for DOS
on or after 12/01/2024

06/06/2024: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

01/23/2024 R16
Revision Effective Date: 01/23/2024
POLICY SPECIFIC DOCUMENTATION REQUIREMENTS:
Removed: “Fabrication of an orthosis using CAD/CAM or similar technology without the

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REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

creation of a positive model with minimal self-adjustment at delivery is considered as

OTS.”
CODING GUIDELINES:
Added: “Use of an additive manufacturing technique, CAD/CAM, or a similar
manufacturing technique is not the sole requirement for a product to be designated as
custom fabricated.”
Removed: “An orthosis that is fabricated from a mold, CAD/CAM, or similar technology
but without the creation of a positive model is considered a prefabricated orthosis.”
Added: “Additive Manufacturing” with a description
Added: “Additive manufacturing is an acceptable custom fabrication technique as long
as it adheres to the CMS DMEPOS Quality Standards, Appendix C.”
Removed: “Use of CAD/CAM or similar technology to create an orthosis without a
positive model of the patient is considered as OTS if the final fitting upon delivery to
the patient requires minimal self-adjustment not requiring expertise as described in this
section.”
Removed: “Use of CAD/CAM or similar technology to create an orthosis without a
positive model of the patient is considered as custom fitted if the final fitting at the
time of delivery to the patient requires more than minimal self-adjustment requiring
expertise as described in this section.”

03/07/2024: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

02/01/2021 R15
Revision Effective Date: 02/01/2021
NON-MEDICAL NECESSITY COVERAGE AND PAYMENT RULES:
Removed: Language that describes prefabricated and custom fabricated orthoses
Revised: “This minimal self-adjustment does not require the services of a certified
orthotist or an individual who has specialized training.” to “This minimal self-
adjustment does not require the services of a certified orthotist or an individual who
has specialized training (as defined in the CODING GUIDELINES section).”
Revised: HCPCS referenced as custom fabricated orthoses, to include “L1900”
Revised: “This information will be corroborated by the functional evaluation in the
orthotist or prosthetist’s records.” to “This information will be corroborated by the
functional evaluation in the orthotist’s records and the method of custom fabrication
should adhere to the DMEPOS Quality Standards, Appendix C.”
MODIFIERS:
Removed: “refer to the CODING GUIDELINES section for additional information”
pertaining to RT and LT modifiers
Added: RT and LT modifier information (relocated from the CODING GUIDELINES
section)
MISCELLANEOUS:
Added: “(Refer to the REPAIR/REPLACEMENT section for more information regarding
billing of L4205 and L4210 HCPCS codes.)”
CODING GUIDELINES:
Added: “CUSTOM FABRICATED”

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REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

Added: “Custom-fabricated additions are appropriate only for custom-fabricated base

orthotics and should not be billed with prefabricated base orthotics” (relocated from the
NON-MEDICAL NECESSITY COVERAGE AND PAYMENT RULES section)
Added: Language that describes custom fabricated orthoses, molded-to-patient-model
custom fabrication, and positive model of the patient
Added: “Specialized Training” and the definition of specialized training
Added: “PREFABRICATED” and language that describes prefabricated orthoses
Removed: “However, for certain types of orthoses, the HCPCS code narrative that best
describes the product does not make a distinction between prefabricated orthoses that
are provided as custom-fit or OTS. These code narratives are correct and must be used
for Medicare billing, without regard to how the product is provided to the beneficiary at
the final delivery.” (Effective March 11, 2021)
Added: “Corresponding HCPCS Code Sets”
Revised: “parallel” to “corresponding” in regard to HCPCS codes
Removed: “(e.g., L4360, L4361, L4386, L4387, L4396 and L4397)” from the sentence
that pertains to corresponding sets of HCPCS codes
Added: HCPCS codes L4360, L4361, L4386, L4387, L4396, and L4397 to a table that
pertains to corresponding sets of HCPCS codes
Added: Information that pertains to the coding of a prefabricated orthosis when a
corresponding HCPCS code set is not available and the unique HCPCS code describes a
custom fitted item, including “Code the product using the unique HCPCS code, if the
product was custom fitted at the time of delivery to the beneficiary” and “Code the
product using a miscellaneous HCPCS code, if the product was not custom fitted at
delivery to the beneficiary and, instead, was provided as OTS to the beneficiary. The
miscellaneous HCPCS code for billing of AFOs and KAFOs is HCPCS code L2999.”
(Effective March 11, 2021)
Revised: “Elastic and Similar Stretchable Materials” to “ELASTIC AND SIMILAR
STRETCHABLE MATERIALS”
Added: “ANKLE-FOOT ORTHOSES,” “KNEE-ANKLE-FOOT ORTHOSES,” “POSITIONING
DEVICES,” “SHOE INSERTS,” “CONCENTRIC TORSION JOINTS,” “WALKING BOOTS,”
“OTHER DEVICES,” and “REPAIR/REPLACEMENT”
Added: Coding guideline information for HCPCS codes L2034, L2036, L2200, L2210,
L2220, L2280, L2330, and L2820
Added: “LOWER EXTREMITY ADDITIONS” and language that describes custom-
fabricated additions
Removed: Language that referred to the HCPCS codes which describe custom
fabricated and prefabricated orthoses
Removed: Language that referred to the HCPCS codes which describe orthoses worn
when a beneficiary is ambulatory, non-ambulatory, or minimally ambulatory
Revised: Language that pertains to shoes, inserts, and shoe modifications that are
integral components of a leg brace and the pertinent HCPCS codes
Removed: RT and LT modifier information

12/07/2023: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

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REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

02/01/2021 R14
Revision Effective Date: 02/01/2021
NON-MEDICAL NECESSITY COVERAGE AND PAYMENT RULES:
Revised: “Braces Benefit” to “braces benefit”
Revised: “Coding Guidelines” to “CODING GUIDELINES”
Revised: “Ankle-Foot Orthosis” to “ankle-foot orthosis”
Revised: “CAD-CAM” to “computer-aided design/computer-aided manufacturing
(CAD/CAM)”
GENERAL REQUIREMENTS:
Revised: “Coding Guidelines” to “CODING GUIDELINES”
Revised: “off-the-self” to “OTS”
MODIFIERS:
Revised: “KX, GA, and GZ MODIFIERS:” to “GA, GZ, KX, LT and RT MODIFIERS:”
Added: Statement regarding use of RT and LT, with reference to CODING GUIDELINES
section for additional information
CODING GUIDELINES:
Revised: Language describing parallel code set availability for identical types of
products
Revised: Coding guideline language for HCPCS codes L1900, L1902, L1904, L1906,
L1907, L1910, L1920, L1930, L1932, L1940, L1945, L1950, L1951, L1960, L1970,
L1971, L1980, L1990, and L2006
Revised: Coding guideline information for HCPCS codes L1910, L1932, and L1951, to
include that there are no additional HCPCS codes for these types of orthoses
Added: Long HCPCS descriptions to coding guidelines for HCPCS codes L2006, L2340,
and L2755
Revised: Language describing the coding of foot orthotics as L-codes or A-codes
Revised: “Durable Medical Equipment” to “durable medical equipment”
Revised: “Braces” to “braces”
Revised: Format of long HCPCS descriptions for HCPCS codes A9270 and L4205

05/26/2022: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

02/01/2021 R13
Revision Effective Date: 02/01/2021
REQUIREMENTS FOR SPECIFIC DMEPOS ITEMS PURSUANT TO FINAL RULE 1713 (84
FED. REG VOL 217):
Removed: “The link will be located here once it is available.”
Added: “The required Face-to-Face Encounter and Written Order Prior to Delivery List is
available here.” with a hyperlink to the list

04/14/2022: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

02/01/2021 R12
Revision Effective Date: 02/01/2021
CODING GUIDELINES:

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REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

Removed: Coding verification review information for HCPCS codes L1906 and L2006
CODING VERIFICATION REVIEW:
Added: Section header and PDAC coding verification review information
Added: Coding verification review information for HCPCS codes L1906 and L2006

03/11/2021: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

02/01/2021 R11
Revision Effective Date: 02/01/2021
NON-MEDICAL NECESSITY COVERAGE AND PAYMENT RULES:
Revised: Prefabricated orthoses (OTS or custom-fit) incorrect coding denial language,
by removing “with a statutory denial”
Added: Definitions of prefabricated and custom fabricated orthoses
Clarified: Billing of custom fabricated additions
CODING GUIDELINES:
Added: Coding guideline information for HCPCS code L2005

11/19/2020: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

10/01/2020 R10
Revision Effective Date: 10/01/2020
MISCELLANEOUS:
Clarified: Custom fabricated items that do not have specific HCPCS codes require
additional information in claim narrative
Added: Statement referring to the LCD-related Standard Documentation Requirements
article for more information
ICD-10 CODES THAT SUPPORT MEDICAL NECESSITY:
Removed: Non-specific ICD-10 codes M24.573 and M24.576 from Group 1 codes
Removed: Non-specific ICD-10 code M14.679 from Group 2 codes

09/24/2020: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

07/01/2020 R9
Revision Effective Date: 07/01/2020
ICD-10 CODES THAT SUPPORT MEDICAL NECESSITY:
Added: ICD-10 diagnosis codes E08.610, E09.610, E10.610, and E11.610 to Group 2
Codes for L4631

06/04/2020: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

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REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

01/01/2020 R8
Revision Effective Date: 01/01/2020
REQUIREMENTS FOR SPECIFIC DMEPOS ITEMS PURSUANT TO FINAL RULE 1713 (84
Fed. Reg Vol 217):
Added: Section and related information based on Final Rule 1713
POLICY SPECIFIC DOCUMENTATION REQUIREMENTS:
Revised: “ordering physician’s” to “treating practitioner’s”
Revised: “physician’s” to “practitioner’s”
Revised: Format of HCPCS code references, from code ‘spans’ to individually-listed
HCPCS
CODING GUIDELINES:
Revised: Format of HCPCS code references, from code ‘spans’ to individually-listed
HCPCS
Added: Coding Guidelines for L1900, L1902, L1904, L1907, L1910, L1920, L1930,
L1932, L1940, L1945, L1950, L1951, L1970, L1971, L1980, and L1990
Revised: L1906 Coding Guideline
Revised: L2006 Coding Guideline per quarterly HCPCS code update
Removed: HCPCS K0903
Added: HCPCS A5514, crosswalk from K0903
Removed: Reference of effective DOS for K0903
Added: Reference of effective DOS for A5514

02/20/2020: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

01/01/2020 R7
Revision Effective Date: 01/01/2020
CODING GUIDELINES:
Added: L2006 Coding Guideline
ICD-10 CODES THAT SUPPORT MEDICAL NECESSITY:
Revised: Section header “ICD-10 Codes that are Covered” updated to “ICD-10 Codes
that Support Medical Necessity”
ICD-10 CODES THAT DO NOT SUPPORT MEDICAL NECESSITY:
Revised: Section header “ICD-10 Codes that are Not Covered” updated to “ICD-10
Codes that DO NOT Support Medical Necessity”

12/19/2019: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

01/01/2019 R6
Revision Effective Date: 01/01/2019
CODING GUIDELINES:
Clarified: Custom fit requirements
Revised: Coding instructions for prefabricated orthoses without distinction of OTS or
custom-fit.
Revised: RT and LT modifier billing instructions (Effective 03/01/2019)
ICD-10 CODES THAT ARE COVERED:

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REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

Added: All diagnosis codes formerly listed in the LCD

ICD-10 CODES THAT ARE NOT COVERED:
Added: Notation excluding unlisted diagnosis codes from coverage for specific HCPCS
codes. Notation that for all other HCPCS codes, diagnoses are not specified.

03/28/2019: At this time 21st Century Cures Act applies to new and revised LCDs
which require comment and notice. This revision is to an article that is not a local
coverage determination.

01/01/2017 R5
Revision Effective Date: 01/01/2017
CODING GUIDELINES:
Revised: Code pairs to accurately reflect parallel codes
Updated: HCPCS code narratives to align with HCPCS code table
Added: Walking boot add-on bundling information

04/05/2018: At this time 21st Century Cures Act applies to new and revised LCDs that
restrict coverage, which require comment and notice. This revision is to an article that
is not a local coverage determination.

01/01/2017 R4 Revision Effective Date: 01/01/2017

NON-MEDICAL NECESSITY COVERAGE AND PAYMENT RULES:
Revised: Brace Benefit explanation to remove reference to “counterforce” that is no
longer applicable
Revised: Prefabricated and off-the-shelf (OTS) “minimal self-adjustment” regulatory
definition discussion to improve consistency with regulatory definition of minimal self-
adjustment
Deleted: A4466
Added: A4467
Added: Instructions for A9285
Added: Policy specific documentation requirements from LCD
CODING GUIDELINES:
Removed: Reference to classification algorithm summary
Revised: OTS and custom-fit definitions to improve consistency with regulatory
definition of “minimal self-adjustment”
Added: Section on coding of elastic and similar materials
Deleted: A4466
Added: A4467
Added A9285
RELATED LOCAL COVERAGE DOCUMENTS:
Added: LCD-related Standard Documentation Requirements Language Article

07/01/2016 R3 Effective July 1, 2016 oversight for DME MAC Articles is the responsibility of CGS
Administrators, LLC 18003 and 17013 and Noridian Healthcare Solutions, LLC 19003
and 16013. No other changes have been made to the Articles.

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REVISION REVISION REVISION HISTORY EXPLANATION
HISTORY HISTORY
DATE NUMBER

01/01/2016 R2 Revision Effective Date: 01/01/2016

CODING GUIDELINES:
Added: L4361 “clerical correction”

10/01/2015 R1 Revision Effective Date: 01/01/2015

NON-MEDICAL NECESSITY COVERAGE AND PAYMENT RULES:
Added: Information for hospital and SNF reimbursement
CODING GUIDELINES:
Added: Reference to classification algorithm summary

Associated Documents
Related Local Coverage Documents

Articles
A55426 - Standard Documentation Requirements for All Claims Submitted to DME MACs
LCDs
L33686 - Ankle-Foot/Knee-Ankle-Foot Orthosis

Related National Coverage Documents

N/A

Statutory Requirements URLs

N/A

Rules and Regulations URLs

N/A

CMS Manual Explanations URLs

N/A

Other URLs

N/A

Public Versions

UPDATED ON EFFECTIVE DATES STATUS

Some older versions have been archived. Please visit the MCD Archive Site to retrieve them.

01/09/2025 01/01/2025 - N/A Currently in Effect (This Version)

05/29/2024 01/23/2024 - 12/31/2024 Superseded

02/29/2024 01/23/2024 - N/A Superseded

12/01/2023 02/01/2021 - 01/22/2024 Superseded

05/18/2022 02/01/2021 - N/A Superseded

Created on 02/13/2025. Page 28 of 29

UPDATED ON EFFECTIVE DATES STATUS

04/07/2022 02/01/2021 - N/A Superseded

03/05/2021 02/01/2021 - N/A Superseded

11/13/2020 02/01/2021 - N/A Superseded

Keywords
N/A

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