ARTHREX INSTRUMENTS (KNEE, GP 3)

ARTHREX INSTRUMENTS (KNEE, GP 3) is an FDA 510(k)-cleared medical device (K925995) 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.