PROPATCH SOFT TISSUE REPAIR MATRIX

PROPATCH SOFT TISSUE REPAIR MATRIX is an FDA 510(k)-cleared medical device (K101587) manufactured by Cryolife, Inc.. 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 September 15, 2010. Regulation: 8.