ACELL UBM SURGICAL MESH ML AND MLPLUS

ACELL UBM SURGICAL MESH ML AND MLPLUS is an FDA 510(k)-cleared medical device (K041140) manufactured by Acell, 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 July 6, 2004. Regulation: 8.