Clearance Summary
MODIFICATION TO V-LOC 180 ABSORBABLE WOUND CLOSURE DEVICE received FDA 510(k) clearance under submission number K091087, sponsored by Surgical Devices, Tyco Healthcare Group LP. 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 2009-04-22.
- Submission: K091087
- Applicant / Sponsor: Surgical Devices, Tyco Healthcare Group LP
- Clearance pathway: Special
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4493
- Decision date: 2009-04-22
Classification & Regulation
This clearance is catalogued under FDA product code GAM and 21 CFR 878.4493, within the General, Plastic Surgery review panel as a Class II device.