Clearance Summary
K3 received FDA 510(k) clearance under submission number K152830, sponsored by Osstem Implant 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 2017-04-20.
- Submission: K152830
- Applicant / Sponsor: Osstem Implant Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class I
- Regulation citation: 21 CFR 872.6640
- Decision date: 2017-04-20
Classification & Regulation
This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.