Clearance Summary
INNOVASIVE DEVICES Y-KNOT SUTURE CLIP received FDA 510(k) clearance under submission number K973313, sponsored by Innovasive Devices, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1997-12-01.
- Submission: K973313
- Applicant / Sponsor: Innovasive Devices, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 1997-12-01
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.