
Surgical Specialties Corporation Dba Angiotech
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QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN is an FDA 510(k)-cleared medical device (K132268) manufactured by Surgical Specialties Corporation 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 August 22, 2013. Regulation: 8.