VITAMESH MACROPOROUS PP SURGICAL MESH

VITAMESH MACROPOROUS PP SURGICAL MESH is an FDA 510(k)-cleared medical device (K060520) manufactured by Proxy Biomedical , Ltd.. 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 March 27, 2006. Regulation: 8.