INTERLOCKING FEMORAL NAILING SYSTEM

INTERLOCKING FEMORAL NAILING SYSTEM is an FDA 510(k)-cleared medical device (K912930) manufactured by Stryker 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 January 12, 1992. Regulation: 8.