
Medical Device Consultants, Inc.
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PARIETEX COMPOSITE (PCO) MESH is an FDA 510(k)-cleared medical device (K002699) manufactured by Medical Device Consultants, 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 February 14, 2001. Regulation: 8.