The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive® Acp System.
Device ID | K191500 |
510k Number | K191500 |
Device Name: | NuVasive® ACP System |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
Contact | Jessica Silverman |
Correspondent | Jessica Silverman NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-06-06 |
Decision Date | 2019-09-03 |
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 |