Clearance Summary
BONALIVE GRANULES AND BONALIVE PLATES received FDA 510(k) clearance under submission number K070055, sponsored by Vivoxid , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2007-06-25.
- Submission: K070055
- Applicant / Sponsor: Vivoxid , Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3930
- Decision date: 2007-06-25
Classification & Regulation
This clearance is catalogued under FDA product code LYC and 21 CFR 872.3930, within the Dental review panel as a Class II device.