PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA

PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA is an FDA 510(k)-cleared medical device (K896853) manufactured by Howmedica 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 May 1, 1990. Regulation: 8.