GLENOID RESURFACING COMPONENT-3M-10816

GLENOID RESURFACING COMPONENT-3M-10816 is an FDA 510(k)-cleared medical device (K831233) manufactured by 3M Company. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 2, 1983. Regulation: 8.