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FDA 510(k), K130498, OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY
FDA 510(k), K130498, OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY
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$149.00 USD
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$149.00 USD
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510(K) Number: K130498
Device Name: OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY
Manufacturer: BACTERIN INTERNATIONAL INC.
Device Classification Name: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
Regulation Number: 888.3045
Classification Product Code: MBP
Date Received: 02/26/2013
Decision Date: 05/31/2013
Regulation Medical Specialty: Orthopedic
Device Name: OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY
Manufacturer: BACTERIN INTERNATIONAL INC.
Device Classification Name: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
Regulation Number: 888.3045
Classification Product Code: MBP
Date Received: 02/26/2013
Decision Date: 05/31/2013
Regulation Medical Specialty: Orthopedic
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