MEDPOR PTERIONAL SURGICAL IMPLANT

MEDPOR PTERIONAL SURGICAL IMPLANT is an FDA 510(k)-cleared medical device (K002586) manufactured by Porex Surgical Products Group. 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 November 16, 2000. Regulation: 8.