ATRIUM PROLITE ULTRA S MESH

ATRIUM PROLITE ULTRA S MESH is an FDA 510(k)-cleared medical device (K070192) manufactured by Atrium Medical Corp.. 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 March 7, 2007. Regulation: 8.