AESCULAP MONOMAX ABSORBABLE SUTURE

AESCULAP MONOMAX ABSORBABLE SUTURE is an FDA 510(k)-cleared medical device (K100876) manufactured by Aesculap, 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 13, 2010. Regulation: 8.