The following data is part of a premarket notification filed by Musculoskeletal Transplant Foundation with the FDA for Dbx Demineralized Bone Matrix Putty.
| Device ID | K091217 |
| 510k Number | K091217 |
| Device Name: | DBX DEMINERALIZED BONE MATRIX PUTTY |
| Classification | Bone Grafting Material, Human Source |
| Applicant | MUSCULOSKELETAL TRANSPLANT FOUNDATION 125 MAY STREET Edison, NJ 08837 |
| Contact | Nancy Bennewitz Joy |
| Correspondent | Nancy Bennewitz Joy MUSCULOSKELETAL TRANSPLANT FOUNDATION 125 MAY STREET Edison, NJ 08837 |
| Product Code | NUN |
| CFR Regulation Number | 872.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-04-27 |
| Decision Date | 2009-10-02 |
| Summary: | summary |