ALPHATEC 2.7 MM CANNULATED CORTICAL LAG SCREW

ALPHATEC 2.7 MM CANNULATED CORTICAL LAG SCREW is an FDA 510(k)-cleared medical device (K923256) 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 October 8, 1992. Regulation: 8.