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FDA 510(k), K080399, DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE
FDA 510(k), K080399, DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE
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510(K) Number: K080399
Device Name: DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE
Manufacturer: MUSCULOSKELETAL TRANSPLANT FOUNDATION
Device Classification Name: filler, bone void, osteoinduction (w/o human growth factor)
Regulation Number: 888.3045
Classification Product Code: MBP
Date Received: 02/14/2008
Decision Date: 10/10/2008
Regulation Medical Specialty: Orthopedic
Device Name: DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE
Manufacturer: MUSCULOSKELETAL TRANSPLANT FOUNDATION
Device Classification Name: filler, bone void, osteoinduction (w/o human growth factor)
Regulation Number: 888.3045
Classification Product Code: MBP
Date Received: 02/14/2008
Decision Date: 10/10/2008
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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