Clearance Summary
QUILL PDO KNOTLESS TISSUE-CLOSURE DEVICE, VARIABLE LOOP DESIGN received FDA 510(k) clearance under submission number K132268, sponsored by Surgical Specialties Corporation Dba Angiotech. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2013-08-23.
- Submission: K132268
- Applicant / Sponsor: Surgical Specialties Corporation Dba Angiotech
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4840
- Decision date: 2013-08-23
Classification & Regulation
This clearance is catalogued under FDA product code NEW and 21 CFR 878.4840, within the General, Plastic Surgery review panel as a Class II device.