QUIXX POSTERIOR RESTORATIVE— 510(k) K040144

Name: FDA 510(k) clearance K040144
Creator: U.S. Food and Drug Administration
Published: 2004-04-01

Substantially Equivalent

Dentsply International

FDA 510(k) clearance K040144 for QUIXX POSTERIOR RESTORATIVE, Substantially Equivalent on 2004-04-01. Applicant: Dentsply International. Device class: 2.

Clearance details

Applicant: Dentsply International
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 2004-01-22
Decision date: 2004-04-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: York, PA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.