FDA 510(k), K051188, GRAFTON DBM

FDA 510(k), K051188, GRAFTON DBM

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510(K) Number: K051188
Device Name: GRAFTON DBM
Manufacturer: OSTEOTECH, INC.
Device Classification Name: bone grafting material, human source
Regulation Number: 872.3930
Classification Product Code: NUN
Date Received: 05/10/2005
Decision Date: 01/03/2006
Regulation Medical Specialty: Dental
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