Clearance Summary
Pekkton Ivory received FDA 510(k) clearance under submission number K170102, sponsored by Cendres+Metaux SA. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2017-11-13.
- Submission: K170102
- Applicant / Sponsor: Cendres+Metaux SA
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3690
- Decision date: 2017-11-13
Classification & Regulation
This clearance is catalogued under FDA product code EBF and 21 CFR 872.3690, within the Dental review panel as a Class II device.