Clearance Summary
IDI IMPLANT SYSTEM received FDA 510(k) clearance under submission number K081806, sponsored by Idi Biomedical, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2008-11-07.
- Submission: K081806
- Applicant / Sponsor: Idi Biomedical, LLC
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2008-11-07
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.