Clearance Summary
Thommen Implant System received FDA 510(k) clearance under submission number K171795, sponsored by Thommen Medical AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-09-29.
- Submission: K171795
- Applicant / Sponsor: Thommen Medical AG
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2017-09-29
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.