Clearance Summary
SIMPLI SIMPLER IMPLANT SYSTEM received FDA 510(k) clearance under submission number K121281, sponsored by Simpler Implant Solutions. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-04-05.
- Submission: K121281
- Applicant / Sponsor: Simpler Implant Solutions
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2013-04-05
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.