MUCOGRAFT— 510(k) K102531

Name: FDA 510(k) clearance K102531
Creator: U.S. Food and Drug Administration
Published: 2010-11-17

Substantially Equivalent

Ed. Geistlich Soehne AG Fur Chemische Industrie

FDA 510(k) clearance K102531 for MUCOGRAFT, Substantially Equivalent on 2010-11-17. Applicant: Ed. Geistlich Soehne AG Fur Chemische Industrie. Device class: 2.

Clearance details

Applicant: Ed. Geistlich Soehne AG Fur Chemische Industrie
Product code: Code NPL
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2010-09-03
Decision date: 2010-11-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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