Clearance Summary
CERAM-PRIME received FDA 510(k) clearance under submission number K002502, sponsored by S & C Polymer GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-11-08.
- Submission: K002502
- Applicant / Sponsor: S & C Polymer GmbH
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3200
- Decision date: 2000-11-08
Classification & Regulation
This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.