FS3000 Suggested L-Codes*: L-1951 & L-2820
Turbomed Orthotics (and any of its respective directors, officers, agents, contractors, interns, suppliers andemployees) 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.
L-1951: Ankle foot orthosis, spiral, (institute of rehabilitative medicine type), plastic or other material, prefabricated, includes fitting and adjustment
L-2820: Addition to lower extremity orthosis, soft interface for molded plastic, below knee section
*Suggested L-Codes are provided as a reference only. It is the responsibility of the practitioner to confirm this information.
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 – Patent pending in Europe & other countries.