Extremity Medical Receives FDA 510(k) Clearance for Axis Charcot Fixation

By Julie A. Vetalice

Extremity Medical announced FDA 510(k) clearance for Axis Charcot, a comprehensive axial fixation system. First cases are scheduled for this month.

This product and the recently-released BioFuse next-gen live-cell bone graft are two of the company's 16 products available globally to treat distal lower and upper extremities. Other 2017 launches include KinematX Total Wrist Arthroplasty, MTP fusion and Jones fracture systems.

Sources: Extremity Medical, LLC; ORTHOWORLD Inc.

Product Labels: Trauma Ankle/Foot/Toe

Tags: 510(k) Clearance, Regulatory