Clearance Summary
Wishbone HA received FDA 510(k) clearance under submission number K211551, sponsored by Wishbone SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-08-20.
- Submission: K211551
- Applicant / Sponsor: Wishbone SA
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3930
- Decision date: 2021-08-20
Classification & Regulation
This clearance is catalogued under FDA product code NPM and 21 CFR 872.3930, within the Dental review panel as a Class II device.