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FDA 510(k), K091217, DBX DEMINERALIZED BONE MATRIX PUTTY
FDA 510(k), K091217, DBX DEMINERALIZED BONE MATRIX PUTTY
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510(K) Number: K091217
Device Name: DBX DEMINERALIZED BONE MATRIX PUTTY
Manufacturer: MUSCULOSKELETAL TRANSPLANT FOUNDATION
Device Classification Name: bone grafting material, human source
Regulation Number: 872.3930
Classification Product Code: NUN
Date Received: 04/27/2009
Decision Date: 10/02/2009
Regulation Medical Specialty: Dental
Device Name: DBX DEMINERALIZED BONE MATRIX PUTTY
Manufacturer: MUSCULOSKELETAL TRANSPLANT FOUNDATION
Device Classification Name: bone grafting material, human source
Regulation Number: 872.3930
Classification Product Code: NUN
Date Received: 04/27/2009
Decision Date: 10/02/2009
Regulation Medical Specialty: Dental
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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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