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FDA 510(k), K113728, SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTY
FDA 510(k), K113728, SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTY
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$149.00 USD
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$149.00 USD
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510(K) Number: K113728
Device Name: SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTY
Manufacturer:
Device Classification Name: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
Regulation Number: 888.3045
Classification Product Code: MBP
Date Received: 12/19/2011
Decision Date: 11/15/2012
Regulation Medical Specialty: Orthopedic
Device Name: SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTY
Manufacturer:
Device Classification Name: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
Regulation Number: 888.3045
Classification Product Code: MBP
Date Received: 12/19/2011
Decision Date: 11/15/2012
Regulation Medical Specialty: Orthopedic
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