FDA 510(k), K103784, DBX DEMINERALIZED BONE MATRIX PUTTY

FDA 510(k), K103784, DBX DEMINERALIZED BONE MATRIX PUTTY

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510(K) Number: K103784
Device Name: DBX DEMINERALIZED BONE MATRIX PUTTY
Manufacturer: MUSCULOSKELETAL TRANSPLANT FOUNDATION
Device Classification Name: filler, bone void, calcium compound
Regulation Number: 888.3045
Classification Product Code: MQV
Date Received: 12/27/2010
Decision Date: 04/13/2011
Regulation Medical Specialty: Orthopedic

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