ANTLIA III WOUND TREATMENT SYSTEM

ANTLIA III WOUND TREATMENT SYSTEM is an FDA 510(k)-cleared medical device (K111333) manufactured by Innovative Therapies, 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 7, 2011. Regulation: 8.