Clearance Summary
FLEXIROOT received FDA 510(k) clearance under submission number K852305, sponsored by Facial Alveodental Implant Rehabilitation, 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 1985-10-16.
- Submission: K852305
- Applicant / Sponsor: Facial Alveodental Implant Rehabilitation, Inc.
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 1985-10-16
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.