XYLOS POROUS SURGICAL MESH

XYLOS POROUS SURGICAL MESH is an FDA 510(k)-cleared medical device (K090880) manufactured by Xylos Corporation. 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 May 26, 2009. Regulation: 8.