The Progressive Orthopaedic Company Total Knee System II

The Progressive Orthopaedic Company Total Knee System II is an FDA 510(k)-cleared medical device (K183344) manufactured by The Progressive Orthopaedic Company, 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 March 17, 2019. Regulation: 8.