Arthrex Nano FiberTak Suture Anchor

Arthrex Nano FiberTak Suture Anchor is an FDA 510(k)-cleared medical device (K254229) 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 March 1, 2026. Regulation: 8.