The following data is part of a premarket notification filed by Musculoskeletal Transplant Foundation with the FDA for Dbx Demineralized Bone Matrix Putty, Dbx Demineralized Bone Matrix Paste.
Device ID | K080399 |
510k Number | K080399 |
Device Name: | DBX DEMINERALIZED BONE MATRIX PUTTY, DBX DEMINERALIZED BONE MATRIX PASTE |
Classification | Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) |
Applicant | MUSCULOSKELETAL TRANSPLANT FOUNDATION 125 MAY STREET Edison, NJ 08837 |
Contact | Nancy B Joy |
Correspondent | Nancy B Joy MUSCULOSKELETAL TRANSPLANT FOUNDATION 125 MAY STREET Edison, NJ 08837 |
Product Code | MBP |
CFR Regulation Number | 888.3045 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-02-14 |
Decision Date | 2008-10-10 |
Summary: | summary |