Clearance Summary
ANCHOR PLUS/NEO ANCHOR PLUS received FDA 510(k) clearance under submission number K053629, sponsored by Kj Meditech. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2006-05-31.
- Submission: K053629
- Applicant / Sponsor: Kj Meditech
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2006-05-31
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.