CPM Medical Consultants Tibial Revision Knee System

CPM Medical Consultants Tibial Revision Knee System is an FDA 510(k)-cleared medical device (K210695) manufactured by Cpm Medical Consultants, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 15, 2021. Regulation: 8.