6.2 VITALLIUM ALLOY CANCELLOUS BONE SCREW

6.2 VITALLIUM ALLOY CANCELLOUS BONE SCREW is an FDA 510(k)-cleared medical device (K944213) manufactured by Howmedica Corp.. 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 8, 1994. Regulation: 8.