PRECISION OSTEOLOCK ACETABULAR COMPONENT

PRECISION OSTEOLOCK ACETABULAR COMPONENT is an FDA 510(k)-cleared medical device (K930275) 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 August 31, 1994. Regulation: 8.