Clearance Summary
K2 Zirkon Blank white classic; K2 Zirkon Blank translucent; K2 Blanks extreme translucent received FDA 510(k) clearance under submission number K173971, sponsored by Yeti Dentalprodukte 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 2018-11-15.
- Submission: K173971
- Applicant / Sponsor: Yeti Dentalprodukte GmbH
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.6660
- Decision date: 2018-11-15
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.