FDA 510(k), K970321, BIO-OSS ANORGANIC BOVINE BONE

FDA 510(k), K970321, BIO-OSS ANORGANIC BOVINE BONE

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510(K) Number: K970321
Device Name: BIO-OSS ANORGANIC BOVINE BONE
Manufacturer: GEISTLICH-PHARMA
Device Classification Name: bone grafting material, synthetic
Regulation Number: 872.3930
Classification Product Code: LYC
Date Received: 01/28/1997
Decision Date: 09/15/1998
Regulation Medical Specialty: Dental
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