ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM))

ADDITION TO THE CONTINUUM KNEE SYSTEM (CKS(TM)) is an FDA 510(k)-cleared medical device (K896542) manufactured by Techmedica, 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 February 14, 1990. Regulation: 8.