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FDA 510(k), K102531, MUCOGRAFT
FDA 510(k), K102531, MUCOGRAFT
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510(K) Number: K102531
Device Name: MUCOGRAFT
Manufacturer: ED. GEISTLICH SOEHNE AG FUR CHEMISCHE INDUSTRIE
Device Classification Name: barrier, animal source, intraoral
Regulation Number: 872.3930
Classification Product Code: NPL
Date Received: 09/03/2010
Decision Date: 11/17/2010
Regulation Medical Specialty: Dental
Device Name: MUCOGRAFT
Manufacturer: ED. GEISTLICH SOEHNE AG FUR CHEMISCHE INDUSTRIE
Device Classification Name: barrier, animal source, intraoral
Regulation Number: 872.3930
Classification Product Code: NPL
Date Received: 09/03/2010
Decision Date: 11/17/2010
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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