Clearance Summary
B&W DENTAL IMPLANT SYSTEM received FDA 510(k) clearance under submission number K120875, sponsored by B&W Srl. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2012-09-07.
- Submission: K120875
- Applicant / Sponsor: B&W Srl
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2012-09-07
Classification & Regulation
This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.