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FDA 510(k), K171050, Geistlich Fibro-Gide
FDA 510(k), K171050, Geistlich Fibro-Gide
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510(K) Number: K171050
Device Name: Geistlich Fibro-Gide
Manufacturer: Geistlich Pharma AG
Device Classification Name: barrier, animal source, intraoral
Regulation Number: 872.3930
Classification Product Code: NPL
Date Received: 04/07/2017
Decision Date: 11/09/2017
Regulation Medical Specialty: Dental
Device Name: Geistlich Fibro-Gide
Manufacturer: Geistlich Pharma AG
Device Classification Name: barrier, animal source, intraoral
Regulation Number: 872.3930
Classification Product Code: NPL
Date Received: 04/07/2017
Decision Date: 11/09/2017
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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