SECOND GENERATION KNEE SYSTEM, FEMORAL, PATELLAR

SECOND GENERATION KNEE SYSTEM, FEMORAL, PATELLAR is an FDA 510(k)-cleared medical device (K895145) manufactured by Orthomet, 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 5, 1990. Regulation: 8.