The following data is part of a premarket notification filed by Zavation Medical Products Llc with the FDA for Ez Plate.
Device ID | K173306 |
510k Number | K173306 |
Device Name: | EZ Plate |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | Zavation Medical Products Llc 220 Lakeland Parkway Flowood, MS 39232 |
Contact | Matt Jones |
Correspondent | Matt Jones Zavation Medical Products Llc 220 Lakeland Parkway Flowood, MS 39232 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-10-18 |
Decision Date | 2018-01-22 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EZ PLATE 87624281 5602863 Live/Registered |
Zavation Medical Products LLC 2017-09-27 |
EZ PLATE 85740004 4556649 Live/Registered |
PVI INDUSTRIES, LLC 2012-09-27 |
EZ PLATE 78206434 2887694 Live/Registered |
RAB LIGHTING INC. 2003-01-23 |