Arthrex Self-Punching PushLock Suture Anchor

Arthrex Self-Punching PushLock Suture Anchor is an FDA 510(k)-cleared medical device (K221099) 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 May 12, 2022. Regulation: 8.