POROUS MORPHIX SUTURE ANCHOR WITH FORCE FIBER SUTURE

POROUS MORPHIX SUTURE ANCHOR WITH FORCE FIBER SUTURE is an FDA 510(k)-cleared medical device (K130467) manufactured by MedShape, 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 December 4, 2013. Regulation: 8.