Arthrex FiberTak Anchors

Arthrex FiberTak Anchors is an FDA 510(k)-cleared medical device (K151230) 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 June 18, 2015. Regulation: 8.