MODIFICATION TO TRELEX MESH SURGICAL MESH

MODIFICATION TO TRELEX MESH SURGICAL MESH is an FDA 510(k)-cleared medical device (K020110) manufactured by Boston Scientific. 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 April 2, 2002. Regulation: 8.