FDA 510(k), K072397, SYNOSS SYNTHETIC BONE GRAFT MATERIAL
FDA 510(k), K072397, SYNOSS SYNTHETIC BONE GRAFT MATERIAL
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510(K) Number: K072397
Device Name: SYNOSS SYNTHETIC BONE GRAFT MATERIAL
Manufacturer:
Device Classification Name: Bone Grafting Material, Synthetic
Regulation Number: 872.3930
Classification Product Code: LYC
Date Received: 08/27/2007
Decision Date: 10/18/2007
Regulation Medical Specialty: Dental
Device Name: SYNOSS SYNTHETIC BONE GRAFT MATERIAL
Manufacturer:
Device Classification Name: Bone Grafting Material, Synthetic
Regulation Number: 872.3930
Classification Product Code: LYC
Date Received: 08/27/2007
Decision Date: 10/18/2007
Regulation Medical Specialty: Dental