Arthrex SwiveLock Suture Anchor

Arthrex SwiveLock Suture Anchor is an FDA 510(k)-cleared medical device (K191226) 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 10, 2019. Regulation: 8.