K2 Zirkon Blank white classic; K2 Zirkon Blank translucent; K2 Blanks extreme translucent— 510(k) K173971

Name: FDA 510(k) clearance K173971
Creator: U.S. Food and Drug Administration
Published: 2018-11-15

Substantially Equivalent

Yeti Dentalprodukte GmbH

FDA 510(k) clearance K173971 for K2 Zirkon Blank white classic; K2 Zirkon Blank translucent; K2 Blanks extreme translucent, Substantially Equivalent on 2018-11-15. Applicant: Yeti Dentalprodukte GmbH. Device class: 2.

Clearance details

Applicant: Yeti Dentalprodukte GmbH
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2017-12-29
Decision date: 2018-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Engen, DE

Download summary PDF View on FDA.gov ↗

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