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Surgical Specialties Corp. Dba Angiotech
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QUILL POLYPROPYLENE KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN is an FDA 510(k)-cleared medical device (K130078) manufactured by Surgical Specialties Corp. Dba Angiotech. 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 27, 2013. Regulation: 8.