ARTHREX BAYONET KNIFE

ARTHREX BAYONET KNIFE is an FDA 510(k)-cleared medical device (K925457) 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 March 3, 1993. Regulation: 8.