Clearance Summary
DB PRECISION IMPLANT SYSTEM, 1000 SERIES W/HAC received FDA 510(k) clearance under submission number K875242, sponsored by Driskell Bioengineering. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1988-02-26.
- Submission: K875242
- Applicant / Sponsor: Driskell Bioengineering
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 1988-02-26
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.