KIRSCHNER NEER-III MODULAR PROXIMAL HUMERUS

KIRSCHNER NEER-III MODULAR PROXIMAL HUMERUS is an FDA 510(k)-cleared medical device (K874643) manufactured by Kirschner Medical 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 January 5, 1988. Regulation: 8.