CONSENSUS PCL SUBSITUTING TIBIAL INSERT

CONSENSUS PCL SUBSITUTING TIBIAL INSERT is an FDA 510(k)-cleared medical device (K953443) manufactured by U.S. Medical Products, 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 April 25, 1996. Regulation: 8.