DIMENSION REVISION TOTAL HIP SYSTEM

DIMENSION REVISION TOTAL HIP SYSTEM is an FDA 510(k)-cleared medical device (K895636) manufactured by Kirschner Medical 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 December 13, 1989. Regulation: 8.