Clearance Summary
Ortholock Anchorage Devices received FDA 510(k) clearance under submission number K202691, sponsored by Craniofacial Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2022-04-28.
- Submission: K202691
- Applicant / Sponsor: Craniofacial Technologies, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2022-04-28
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.