BIOMESH P1 AND BIOMESH PLUG AND PATCH

BIOMESH P1 AND BIOMESH PLUG AND PATCH is an FDA 510(k)-cleared medical device (K002479) manufactured by Cousin Biotech S.A.R.L. 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 October 18, 2000. Regulation: 8.