U.S. TYPE CRUCIATE SLOT BONE SCREW

U.S. TYPE CRUCIATE SLOT BONE SCREW is an FDA 510(k)-cleared medical device (K903254) manufactured by Onyx Medical 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 August 8, 1990. Regulation: 8.