ARTHREX TIBIAL TUNNEL CANNULA

ARTHREX TIBIAL TUNNEL CANNULA is an FDA 510(k)-cleared medical device (K930152) 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 10, 1994. Regulation: 8.