NEOTRACT ANCHOR SYSTEM MODEL TAS400

NEOTRACT ANCHOR SYSTEM MODEL TAS400 is an FDA 510(k)-cleared medical device (K102028) manufactured by Neotract, 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 August 3, 2010. Regulation: 8.