Clearance Summary
OPUS SMARTSTITCH SUTURE DEVICE received FDA 510(k) clearance under submission number K070671, sponsored by Arthrocare Corp.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2007-04-06.
- Submission: K070671
- Applicant / Sponsor: Arthrocare Corp.
- Clearance pathway: Special
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2007-04-06
Classification & Regulation
This clearance is catalogued under FDA product code OCW and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.