Clearance Summary
Implance Dental Implant System, Implance Dental Abutment System received FDA 510(k) clearance under submission number K160221, sponsored by Ags Medikal Urunleri Ith. Ihr. Tic. Ltd. Sti.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-09-12.
- Submission: K160221
- Applicant / Sponsor: Ags Medikal Urunleri Ith. Ihr. Tic. Ltd. Sti.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2016-09-12
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.