Arthrex Knee FiberTak® Button Suture Anchor

Arthrex Knee FiberTak® Button Suture Anchor is an FDA 510(k)-cleared medical device (K232973) 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 November 14, 2023. Regulation: 8.