INSET PATELLAR COMPONENT

INSET PATELLAR COMPONENT is an FDA 510(k)-cleared medical device (K904300) manufactured by Johnson & Johnson Orthopaedics, 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 October 16, 1990. Regulation: 8.