POROUS GENESIS PATELLAR AND STEMLESS TIBIAL COMP.

POROUS GENESIS PATELLAR AND STEMLESS TIBIAL COMP. is an FDA 510(k)-cleared medical device (K890132) manufactured by Richards Medical Co., Inc.. 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 18, 1989. Regulation: 8.