ZENO PMMA DISC— 510(k) K080182

Name: FDA 510(k) clearance K080182
Creator: U.S. Food and Drug Administration
Published: 2008-04-08

Substantially Equivalent

Wieland Dental + Technik GmbH & Co. KG

FDA 510(k) clearance K080182 for ZENO PMMA DISC, Substantially Equivalent on 2008-04-08. Applicant: Wieland Dental + Technik GmbH & Co. KG. Device class: 2.

Clearance details

Applicant: Wieland Dental + Technik GmbH & Co. KG
Product code: Code EBG
Device class: Class 2
Regulation: 21 CFR 872.3770
Advisory panel: Dental
Date received: 2008-01-25
Decision date: 2008-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pforzheim, DE

Download summary PDF View on FDA.gov ↗

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