STRYKER WEDGE INTERFERENCE SCREW SYSTEM

STRYKER WEDGE INTERFERENCE SCREW SYSTEM is an FDA 510(k)-cleared medical device (K972233) manufactured by Stryker Endoscopy. 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 4, 1997. Regulation: 8.