RSP GLENOID BASEPLATE POROUS COATED

RSP GLENOID BASEPLATE POROUS COATED is an FDA 510(k)-cleared medical device (K112069) manufactured by Encore Medical L.P.. 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 14, 2011. Regulation: 8.