BUECHEL-PAPPAS HUMERAL STEM COMPONENT

BUECHEL-PAPPAS HUMERAL STEM COMPONENT is an FDA 510(k)-cleared medical device (K904880) manufactured by Endotec, 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 January 27, 1991. Regulation: 8.