F-230 POROUS FEMORAL HIP STEM (CEMENTLESS)

F-230 POROUS FEMORAL HIP STEM (CEMENTLESS) is an FDA 510(k)-cleared medical device (K941612) manufactured by Implex 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 July 5, 1995. Regulation: 8.