MESO TENDON MATRIX

MESO TENDON MATRIX is an FDA 510(k)-cleared medical device (K133169) manufactured by Kensey Nash Corporation Dba Dsm Biomedical. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 19, 2013. Regulation: 8.