The following data is part of a premarket notification filed by Depuy Mitek, A Johnson & Johnson Company with the FDA for Various.
| Device ID | K112417 |
| 510k Number | K112417 |
| Device Name: | VARIOUS |
| Classification | Fastener, Fixation, Nondegradable, Soft Tissue |
| Applicant | DEPUY MITEK, A JOHNSON & JOHNSON COMPANY 325 PARAMOUNT DR. Raynham, MA 02767 |
| Contact | Deep Pal |
| Correspondent | Deep Pal DEPUY MITEK, A JOHNSON & JOHNSON COMPANY 325 PARAMOUNT DR. Raynham, MA 02767 |
| Product Code | MBI |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-08-23 |
| Decision Date | 2012-01-13 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() VARIOUS 85570019 4229680 Live/Registered |
Various, Inc. 2012-03-15 |
![]() VARIOUS 75495306 2318030 Dead/Cancelled |
SAVA, gumarska in kemicna industrija, d.d. 1998-06-02 |