ALPHATEC CANNULATED BONE SCREWS

ALPHATEC CANNULATED BONE SCREWS is an FDA 510(k)-cleared medical device (K914004) manufactured by Alphatec Mfg., 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 December 4, 1991. Regulation: 8.