Clearance Summary
OsseOne Dental Implant System received FDA 510(k) clearance under submission number K182293, sponsored by Synoross Dba Osseone. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2019-02-15.
- Submission: K182293
- Applicant / Sponsor: Synoross Dba Osseone
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2019-02-15
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.