Arthrex Knotless AC Repair Devices

Arthrex Knotless AC Repair Devices is an FDA 510(k)-cleared medical device (K220947) 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 5, 2022. Regulation: 8.