IMPLEX CONTINUUM POROUS PATELLAR

IMPLEX CONTINUUM POROUS PATELLAR is an FDA 510(k)-cleared medical device (K971789) 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 July 23, 1997. Regulation: 8.