SMR 3-PEGS GLENOIDS

SMR 3-PEGS GLENOIDS is an FDA 510(k)-cleared medical device (K130642) manufactured by Lima Corporate S.P.A.. 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 11, 2013. Regulation: 8.