Clearance Summary
BVI SLING received FDA 510(k) clearance under submission number K002233, sponsored by Bio-Vascular, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2000-10-13.
- Submission: K002233
- Applicant / Sponsor: Bio-Vascular, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.3300
- Decision date: 2000-10-13
Classification & Regulation
This clearance is catalogued under FDA product code PAJ and 21 CFR 878.3300, within the General, Plastic Surgery review panel as a Class II device.