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 |