XTERN Suggested L Code **PDAC VALIDATED** L1951
L1951: Ankle foot orthosis, spiral, (institute of rehabilitative medicine type), plastic or other material, prefabricated, includes fitting and adjustment.
*Suggested L Codes: The responsibility for accurate coding lies with the patient care facility that selects the product, fits the patient, and bills for the service.
Turbomed Orthotics (and any of its respective directors, officers, agents, contractors, interns, suppliers and employees) will not be liable for any damages, losses or causes of action of any nature arising from any use of any of the informations or the provision of these above informations. It should be noted that, regardless of the source of coding information and guidelines, the final responsibility for correct coding, within all established laws, rules, standards, and practices is the sole responsibility of the facility and/or person who is submitting the claim.
Health Canada Medical Device Establishment License No 6354 Class I – CE Class I Medical Device – FDA Registration No: 3011816892 – Medical Device Listing no: D246429 - U.S. Patent No.8529484 – Canadian Patent 2692534 – European Patent EP2533734 - International Patent Pending.