
Osteogenics Biomedical, Inc.
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CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC is an FDA 510(k)-cleared medical device (K003028) manufactured by Osteogenics Biomedical, 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 November 23, 2000. Regulation: 8.