Clearance Summary
CORTEX DENTAL IMPLANT SYSTEM received FDA 510(k) clearance under submission number K090709, sponsored by Cortex Dental Implants Industries , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2009-07-07.
- Submission: K090709
- Applicant / Sponsor: Cortex Dental Implants Industries , Ltd.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2009-07-07
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.