Clearance Summary
BIOGRAN BIOACTIVE GLASS SYNTHETIC BONE GRAFT MATERIAL received FDA 510(k) clearance under submission number K952922, sponsored by Orthovita Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1995-12-19.
- Submission: K952922
- Applicant / Sponsor: Orthovita Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3930
- Decision date: 1995-12-19
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.