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News

September 3, 2019

XTERN AFO Get's PDAC Validation - L1951

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Products
Turbomed XTERN
  • XTERN CLASSIC AFO
  • AT-X ASSESSMENT TOOL
  • Parts & Options
  • Pricing
  • How to get the XTERN?
Kits
  • Large Assembly
  • Medium Assembly
  • Small Assembly
  • Pediatric Assembly
Tools
  • Sizing Chart & Kits Selection
  • Assessment Tool AT-X
Options
  • Ankle strap Small-Medium-Large
  • EXTENSION STOPPER KIT 30-40-45 mm (NEW)
  • HEEL BUMPER KIT
Information
  • XTERN AFO -General Information Flyer
  • XTERN PEDIATRIC AFO -General Information Flyer
  • Thermoforming Guidelines
  • Fitting Instruction Footwear
  • CALF PAD & STRAP KIT INSTALLATION
  • Patient Information
  • PDAC validated!
Photos
Videos
FAQ
Contact Us
About Us
  • Our Team
  • Our History
  • News

*HCPCS Code  L1951 PDAC VALIDATED
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.

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© 2023 Turbomed Orthotics. All Rights Reserved.

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.