INTERMEDICS' NATURAL-KNEE(R) REVISION SYSTEM

INTERMEDICS' NATURAL-KNEE(R) REVISION SYSTEM is an FDA 510(k)-cleared medical device (K873602) manufactured by Intermedics Orthopedics. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 26, 1988. Regulation: 8.