The following data is part of a premarket notification filed by Howmedica Osteonics with the FDA for Bonesource Bvf.
Device ID | K031435 |
510k Number | K031435 |
Device Name: | BONESOURCE BVF |
Classification | Filler, Bone Void, Calcium Compound |
Applicant | HOWMEDICA OSTEONICS 59 ROUTE 17 Allendale, NJ 07401 -1677 |
Contact | Debra Bing |
Correspondent | Debra Bing HOWMEDICA OSTEONICS 59 ROUTE 17 Allendale, NJ 07401 -1677 |
Product Code | MQV |
CFR Regulation Number | 888.3045 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-05-06 |
Decision Date | 2003-08-04 |
Summary: | summary |