Clearance Summary
Ritter Dental Implant System received FDA 510(k) clearance under submission number K160475, sponsored by Ritter Implants GmbH & Co. KG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-12-14.
- Submission: K160475
- Applicant / Sponsor: Ritter Implants GmbH & Co. KG
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2016-12-14
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.