Arthrex 2.5 mm Tenodesis Screw

Arthrex 2.5 mm Tenodesis Screw is an FDA 510(k)-cleared medical device (K183395) 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 April 16, 2019. Regulation: 8.