IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS

IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS is an FDA 510(k)-cleared medical device (K932923) 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 May 2, 1994. Regulation: 8.