FDA 510(k), K122894, GEISTLICH BIO-OSS, GEISTLICH BIO-OSS COLLAGEN, GEISTLICH COMBI-KIT COLLAGEN, GEISTLICH PERIO SYSTEM COMBI PACK, GEISTLIC

FDA 510(k), K122894, GEISTLICH BIO-OSS, GEISTLICH BIO-OSS COLLAGEN, GEISTLICH COMBI-KIT COLLAGEN, GEISTLICH PERIO SYSTEM COMBI PACK, GEISTLIC

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510(K) Number: K122894
Device Name: GEISTLICH BIO-OSS, GEISTLICH BIO-OSS COLLAGEN, GEISTLICH COMBI-KIT COLLAGEN, GEISTLICH PERIO SYSTEM COMBI PACK, GEISTLIC
Manufacturer: DANIEL A KRACOV
Device Classification Name: Bone Grafting Material, Animal Source
Regulation Number: NPM
Classification Product Code: 09/20/2012
Date Received: 02/15/2013
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
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