Clearance Summary
HOLLOW SCREW IMPLANTS 6MM, 14MM, 16MM received FDA 510(k) clearance under submission number K920768, sponsored by The Straumann 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 1992-04-21.
- Submission: K920768
- Applicant / Sponsor: The Straumann Co.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 1992-04-21
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.