CAPITELLO-CONDYLAR TOTAL ELBOW PROSTHESIS

CAPITELLO-CONDYLAR TOTAL ELBOW PROSTHESIS is an FDA 510(k)-cleared medical device (K983141) manufactured by Johnson & Johnson Professionals, 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 November 5, 1998. Regulation: 8.