HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM

HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM is an FDA 510(k)-cleared medical device (K954559) manufactured by Howmedica Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 11, 1996. Regulation: 8.