ARTHREX CORKSCREW FT III SUTURE ANCHOR WITH THREE #2 SUTURES

ARTHREX CORKSCREW FT III SUTURE ANCHOR WITH THREE #2 SUTURES is an FDA 510(k)-cleared medical device (K062679) 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 September 26, 2006. Regulation: 8.