ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE— 510(k) K093894

Name: FDA 510(k) clearance K093894
Creator: U.S. Food and Drug Administration
Published: 2010-03-03

Substantially Equivalent

Anthogyr

FDA 510(k) clearance K093894 for ANTHOGYR IMPULSION IMPLANTOLOGY CONTRA-ANGLE, Substantially Equivalent on 2010-03-03. Applicant: Anthogyr. Device class: 1.

Clearance details

Applicant: Anthogyr
Product code: Code EFA
Device class: Class 1
Regulation: 21 CFR 872.4200
Advisory panel: Dental
Date received: 2009-12-18
Decision date: 2010-03-03
Decision: Substantially Equivalent
Clearance type: Special
Location: Sallanches, FR

Download summary PDF View on FDA.gov ↗

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