The following data is part of a premarket notification filed by Bacterin International Inc. with the FDA for Osteoselect Demineralized Bone Matrix Putty.
Device ID | K130498 |
510k Number | K130498 |
Device Name: | OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTY |
Classification | Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) |
Applicant | BACTERIN INTERNATIONAL INC. 600 CRUISER LN. Belgrade, MT 59714 |
Contact | Howard L Schrayer |
Correspondent | Howard L Schrayer BACTERIN INTERNATIONAL INC. 600 CRUISER LN. Belgrade, MT 59714 |
Product Code | MBP |
CFR Regulation Number | 888.3045 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-02-26 |
Decision Date | 2013-05-31 |
Summary: | summary |