TI. ALLOY 2.0 MM CORTEX SCREW

TI. ALLOY 2.0 MM CORTEX SCREW is an FDA 510(k)-cleared medical device (K952272) manufactured by Synthes (Usa). This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 30, 1995. Regulation: 8.