SMITH & NEPHEW GLOBAL FEMORAL HEAD TRIALS

SMITH & NEPHEW GLOBAL FEMORAL HEAD TRIALS is an FDA 510(k)-cleared medical device (K132435) manufactured by Smith & Nephew, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 21, 2013. Regulation: 8.