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 |