Geistlich Fibro-Gide— 510(k) K171050

Substantially Equivalent

Geistlich Pharma AG

FDA 510(k) clearance K171050 for Geistlich Fibro-Gide, Substantially Equivalent on 2017-11-09. Applicant: Geistlich Pharma AG. Device class: 2.

Clearance details

Applicant: Geistlich Pharma AG
Product code: Code NPL
Device class: Class 2
Regulation: 21 CFR 872.3930
Advisory panel: Dental
Date received: 2017-04-07
Decision date: 2017-11-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wolhusen, Lu, CH

Download summary PDF View on FDA.gov ↗

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