Arthrex AlloSync PushLock Suture Anchor

Arthrex AlloSync PushLock Suture Anchor is an FDA 510(k)-cleared medical device (K233971) 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 3, 2024. Regulation: 8.