The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive® Vuepoint® Ii Oct System.
Device ID | K180198 |
510k Number | K180198 |
Device Name: | NuVasive® VuePoint® II OCT System |
Classification | Orthosis, Cervical Pedicle Screw Spinal Fixation |
Applicant | NuVasive, Incorporated 7475 Lusk Boulevard San Diego, CA 92121 |
Contact | Michelle Cheung |
Correspondent | Michelle Cheung NuVasive, Incorporated 7475 Lusk Boulevard San Diego, CA 92121 |
Product Code | NKG |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-01-24 |
Decision Date | 2018-03-15 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NUVASIVE 76298757 2818737 Live/Registered |
NUVASIVE, INC. 2001-08-10 |
NUVASIVE 75822001 2541247 Live/Registered |
NUVASIVE, INC. 1999-10-13 |