FDA 510(k), K132071, BIOACTIVE BONE GRAFT PUTTY

FDA 510(k), K132071, BIOACTIVE BONE GRAFT PUTTY

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510(K) Number: K132071
Device Name: BIOACTIVE BONE GRAFT PUTTY
Manufacturer: BIOSTRUCTURES, LLC
Device Classification Name: filler, bone void, calcium compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 07/03/2013
Decision Date: 01/10/2014
Regulation Medical Specialty: Orthopedic
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