Clearance Summary
A Plus Internal Fixture System received FDA 510(k) clearance under submission number K152786, sponsored by T-Plus Implant Tech. Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2016-06-07.
- Submission: K152786
- Applicant / Sponsor: T-Plus Implant Tech. Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2016-06-07
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.