
Davis & Geck, Inc.
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POLYPROPYLENE MESH (VARIOUS SIZES) is an FDA 510(k)-cleared medical device (K962971) manufactured by Davis & Geck, 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 September 15, 1996. Regulation: 8.