Clearance Summary
VITA YZ ST and VITA YZ XT received FDA 510(k) clearance under submission number K180703, sponsored by Vita Zahnfabrik H.Rauter GmbH Co.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2018-08-01.
- Submission: K180703
- Applicant / Sponsor: Vita Zahnfabrik H.Rauter GmbH Co.
- Clearance pathway: Abbreviated
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2018-08-01
Classification & Regulation
This clearance is catalogued under FDA product code EIH and 21 CFR 872.6660, within the Dental review panel as a Class II device.