ARTHREX SUTURE GRAFTING KIT

ARTHREX SUTURE GRAFTING KIT is an FDA 510(k)-cleared medical device (K041553) manufactured by Arthrex, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 9, 2004. Regulation: 8.