Clearance Summary
OBS Anchorage Screw, Biokey Anchorage Screw received FDA 510(k) clearance under submission number K202278, sponsored by Bomei Co, Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-01-08.
- Submission: K202278
- Applicant / Sponsor: Bomei Co, Ltd.
- Clearance pathway: Special
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2021-01-08
Classification & Regulation
This clearance is catalogued under FDA product code OAT and 21 CFR 872.3640, within the Dental review panel as a Class II device.