Take the Prior Authorization Survey

Prior Authorization Lookup Tool

Determine which HCPCS codes require a Prior Authorization

    Loading

Enter HCPCS Code:

  
 

Prior Authorization for Orthoses

The CMS Final Rule (42 CFR §§ 405 and 414), issued in 2016, established a Prior Authorization (PA) program for selected DMEPOS items that have historically demonstrated high rates of unnecessary utilization. Implementation of prior authorization for specific orthotic HCPCS codes began on April 13, 2022, with a phased-in rollout involving five codes. The PA requirements were further expanded on August 12, 2024, to include six additional orthotic HCPCS codes, while one previously included code was removed from the program.

Beginning April 13, 2026, PA will be required nationwide for HCPCS codes L0651, L1844, L1846, L1852, and L1932. Suppliers may submit requests for review beginning March 30, 2026.

Prior Authorization Timelines

Policy Initial Review Decision Timeframe Expedited Review Decision Timeframe PAR Decision Valid
Orthoses 5 business days (not to exceed 7 calendar days) 2 business days 60 days

Access the below related information from this page.

HCPCS Requiring Prior Authorization (PA)

HCPCS EFFECTIVE DATE DESCRIPTION
L0631 August 12, 2024 Lumbar-sacral orthosis, sagittal control, with rigid anterior and posterior panels, posterior extends from sacrococcygeal junction to t-9 vertebra, produces intracavitary pressure to reduce load on the intervertebral discs, includes straps, closures, may include padding, shoulder straps, pendulous abdomen design, prefabricated item that has been trimmed, bent, molded, assembled, or otherwise customized to fit a specific patient by an individual with expertise.
L0637 August 12, 2024 Lumbar-sacral orthosis, sagittal-coronal control, with rigid anterior and posterior frame/panels, posterior extends from sacrococcygeal junction to t-9 vertebra, lateral strength provided by rigid lateral frame/panels, produces intracavitary pressure to reduce load on intervertebral discs, includes straps, closures, may include padding, shoulder straps, pendulous abdomen design, prefabricated item that has been trimmed, bent, molded, assembled, or otherwise customized to fit a specific patient by an individual with expertise.
L0639 August 12, 2024 Lumbar-sacral orthosis, sagittal-coronal control, rigid shell(s)/panel(s), posterior extends from sacrococcygeal junction to t-9 vertebra, anterior extends from symphysis pubis to xyphoid, produces intracavitary pressure to reduce load on the intervertebral discs, overall strength is provided by overlapping rigid material and stabilizing closures, includes straps, closures, may include soft interface, pendulous abdomen design, prefabricated item that has been trimmed, bent, molded, assembled, or otherwise customized to fit a specific patient by an individual with expertise.
L0648 April 13, 2022 Lumbar-Sacral Orthosis, Sagittal Control, With Rigid Anterior And Posterior Panels, Posterior Extends From Sacrococcygeal Junction To T-9 Vertebra, Produces Intracavitary Pressure To Reduce Load On The Intervertebral Discs, Includes Straps, Closures, May Include Padding, Shoulder Straps, Pendulous Abdomen Design, Prefabricated, Off-The-Shelf
L0650 April 13, 2022 Lumbar-Sacral Orthosis, Sagittal-Coronal Control, With Rigid Anterior And Posterior Frame/Panel(S), Posterior Extends From Sacrococcygeal Junction To T-9 Vertebra, Lateral Strength Provided By Rigid Lateral Frame/Panel(S), Produces Intracavitary Pressure To Reduce Load On Intervertebral Discs, Includes Straps, Closures, May Include Padding, Shoulder Straps, Pendulous Abdomen Design, Prefabricated, Off-The-Shelf
L0651 April 13, 2026 Lumbar-sacral orthosis (LSO), sagittal-coronal control, rigid shell(s)/panel(s), posterior extends from sacrococcygeal junction to t-9 vertebra, anterior extends from symphysis pubis to xyphoid, produces intracavitary pressure to reduce load on the intervertebral discs, overall strength is provided by overlapping rigid material and stabilizing closures, includes straps, closures, may include soft interface, pendulous abdomen design, prefabricated, off-the-shelf
L1832 April 13, 2022 Knee Orthosis, Adjustable Knee Joints (Unicentric Or Polycentric), Positional Orthosis, Rigid Support, Prefabricated Item That Has Been Trimmed, Bent, Molded, Assembled, Or Otherwise Customized To Fit A Specific Patient By An Individual With Expertise
L1843 August 12, 2024 Knee orthosis, single upright, thigh and calf, with adjustable flexion and extension joint (unicentric or polycentric), medial-lateral and rotation control, with or without varus/valgus adjustment, prefabricated item that has been trimmed, bent, molded, assembled, or otherwise customized to fit a specific patient by an individual with expertise.
L1844 April 13, 2026

Knee orthosis, single upright, thigh and calf,

with adjustable flexion and extension joint

(unicentric or polycentric), medial-lateral and

rotation control, with or without varus/valgus

adjustment, custom fabricated

L1845 August 12, 2024 Knee orthosis, double upright, thigh and calf, with adjustable flexion and extension joint (unicentric or polycentric), medial-lateral and rotation control, with or without varus/valgus adjustment, prefabricated item that has been trimmed, bent, molded, assembled, or otherwise customized to fit a specific patient by an individual with expertise.
L1846 April 13, 2026

Knee orthosis, double upright, thigh and calf,

with adjustable flexion and extension joint

(unicentric or polycentric), medial-lateral and

rotation control, with or without varus/valgus

adjustment, custom fabricated

L1851 April 13, 2022 Knee Orthosis (Ko), Single Upright, Thigh And Calf, With Adjustable Flexion And Extension Joint (Unicentric Or Polycentric), Medial-Lateral And Rotation Control, With Or Without Varus/Valgus Adjustment, Prefabricated, Off The-Shelf
L1852 April 13, 2026

Knee orthosis, double upright, thigh and calf,

with adjustable flexion and extension joint

(unicentric or polycentric), medial- lateral and

rotation control, with or without varus/valgus

adjustment, prefabricated, off-the-shelf

L1932 April 13, 2026

Ankle foot orthosis, rigid anterior tibial section,

total carbon fiber or equal material, refabricated item that has been trimmed, bent, molded, assembled, or otherwise customized to fit a specific patient by an individual with expertise

L1951 August 12, 2024 Ankle foot orthosis, spiral, (Institute of Rehabilitative Medicine type), plastic or other material, prefabricated, includes fitting and adjustment.

Documentation Required to Include in Submission to Obtain Prior Authorization (PA)

Documentation must be submitted with the PA coversheet for fax, mail, or electronic submission of medical documentation (esMD). For Noridian Medicare Portal (NMP) submissions, complete all required fields. A coversheet is not required for NMP submission.

Bilateral orthoses - Please note that bilateral orthoses PA requests can be submitted on the same request; however, the medical necessity documentation must support the need for bilateral braces. This can be done on the order with a quantity of two or indicating right and left side, or the medical record documentation indicating the need for two orthoses.

Mirror image codes - PA requests can be submitted on the same request if submitting a prior authorization for a mirror code orthosis because it is unknown whether an off-the-shelf or custom fit brace will be needed until the time of delivery. This should be indicated on the supporting documentation submitted for the prior authorization.

To ensure process efficiency, ensure all components are completed and included within the submission and submitted to the correct jurisdiction.

L0651, L1852, L1932

  • Medical record documentation justifying payment
    • The medical record is not limited to treating practitioner's office records but may include records from hospitals, nursing facilities, home health agencies, other healthcare professionals, etc. (not all-inclusive).
  • Standard Written Order (SWO)

L0631, L0637, L0639, L0648, L0650, L1832, L1843, L1844, L1845, L1846, L1851, L1951

  • Face-to-Face Encounter (F2F)
    • The face-to-face encounter must support payment for the item(s) ordered/prescribed, and be documented in the pertinent portion of the medical record (for example, history, physical examination, diagnostic tests, summary of findings, progress notes, treatment plans or other sources of information that may be appropriate). The supporting documentation must include subjective and objective beneficiary specific information used for diagnosing, treating, or managing a clinical condition for which the DMEPOS is ordered.
  • Written Order Prior to Delivery (WOPD)
    • Must be completed within six (6) months after the required face-to-face encounter

See the Standard Documentation Requirements Article (A55426) for all requirements

Methods of Submission

Expedited Request Guidelines

Expedited requests must include supporting medical documentation demonstrating that the standard five-business-day review timeframe could jeopardize the beneficiary's health or well-being. The physician must clearly state this concern and provide rationale within the submitted documentation

When documentation does not support the above guidelines, expedited requests will be reviewed per the standard timeframe (5-business days).

Situations to Bypass Prior Authorization

Due to the need for certain patients to receive an orthosis in an acute/emergent situation or after surgery, that may otherwise be subject to prior authorization, when the 2-day expedited review would delay care and risk the health or life of the beneficiary, prior authorization may be suspended.

  • The acute/emergent situation must be documented within the physician's records
  • Claims will be billed using the ST modifier and may be subject to a prepayment review.

Prepayment Reviews When Bypassing Prior Authorization

  • When a prepayment review occurs, additional documentation is requested in a letter. The supplier has 45 days from the date of the letter to submit the documentation. Once the documentation is received, the DME MAC has 30 days to review for a decision.

Avoid Request Rejections

There are several circumstances in which a prior authorization (PA) request may be rejected without being reviewed. Ensuring the PA coversheet is completed accurately, all required information is correctly entered into the Noridian Medicare Portal (NMP), and a thorough intake process is followed can help reduce these occurrences.

Common reasons for rejection include:

  • The HCPCS code submitted does not require prior authorization.
  • The beneficiary does not reside within the applicable jurisdiction.
  • The request is a duplicate of a previously submitted prior authorization.
  • There is already an affirmative, identical, prior authorization request within the validation period on file.

Affirmative and Non-Affirmative Decisions

After the PA submission goes through the medical review process, the supplier will receive a decision letter.

When applicable, the prior authorization decision and corresponding claim information may remain with the beneficiary (i.e., the prior authorization decision identified via a Unique Tracking Number, or UTN, may transfer between suppliers and jurisdictions). CMS assumes such transfers would be made in accordance with applicable privacy laws.

Affirmative

Based on the review, it was determined the beneficiary meets the medical necessity requirements established by Medicare for the orthotic item requested.

Process once an affirmed decision has been received:

  • Deliver orthotic and obtain proof of delivery
  • Submit the claim
    • Include the 14-byte Unique Tracking Number (UTN), provided within the decision letter, as indicated below. Each HCPCS code has separate UTN
    • If billing electronically, include UTN in loop 2300 REF02 (REF01 = G1) or loop 2400 REF02 (REF01 = G1), one UTN submitted per claim line
  • If billing on CMS-1500 Claim Form, include UTN in Item 23, one UTN per claim form

Although a Prior Authorization (PA) Affirmation Decision is considered provisional, it offers a significant advantage by allowing suppliers and beneficiaries to determine whether the submitted documentation meets Medicare's coverage criteria before the item is delivered.

This process also enables the DME MAC to identify any additional information that may be required and to provide feedback before an initial claim determination is made.

It is important to note that an affirmative PA decision does not prevent other entities from conducting subsequent reviews of the claim.

Non-Affirmative

Based on the review outcome, a supplier may proceed with one of the following options:

  1. Resubmit the Prior Authorization (PA) Request
    1. Review the decision and submit a PA resubmission.
    2. Provide any missing or clarifying documentation as needed.
    3. Submit an unlimited number of resubmissions.
  2. Deliver the Orthotic and Submit the Claim for Denial
    1. Issue an Advance Beneficiary Notice of Non-coverage (ABN) prior to delivery, when appropriate.
    2. File an appeal after the denial, if desired.
  3. Decline to Deliver or Bill for the Item

Decision Letters

Treating practitioners involved in the submission of a prior authorization may request a copy of the decision letter.

  • Treating practitioner requesting the letter must be able to demonstrate a legitimate, specific need for information requested
  • Request may be sent in with PA request or separately

Still Have Questions?

Call the Supplier Contact Center or Interactive Voice Response (IVR).

Resources

 

Last Updated Feb 04 , 2026