A custom-fabricated AFO (e.g., L1970) is made from raw materials over a model of the patient's extremity, ensuring a unique and precise fit. A prefabricated AFO (e.g., L1971) is a pre-manufactured item that is trimmed, bent, and/or molded to fit the patient. The distinction is in the manufacturing process and the degree of customization required.

HCPCS code L1971: Ankle foot orthosis with ankle joint, prefabricated
Ensure that you meet the description and billing requirements for HCPCS code L1971 in our short guide to properly use and bill the aforementioned code.
Frequently asked questions
Yes—minor modifications such as trimming or bending a prefabricated device for proper fit, provided they don’t cross into full custom fabrication, still qualify under L1971. Custom fabrication transitions billing to L1970.
Required documentation includes: supporting diagnoses (neuromuscular weakness, gait instability, etc.), functional limitation assessment, justification for a jointed prefabricated AFO over alternatives, details of fitting and adjustment, and compliance with LCD “reasonable and necessary” criteria.
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