INTERLOCKING TIBIAL NAILING SYSTEM

INTERLOCKING TIBIAL NAILING SYSTEM is an FDA 510(k)-cleared medical device (K915435) 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 March 1, 1992. Regulation: 8.