Arthrex Minimally Invasive Ankle Fusion Plate

Arthrex Minimally Invasive Ankle Fusion Plate is an FDA 510(k)-cleared medical device (K190953) manufactured by Arthrex, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 15, 2019. Regulation: 8.