The following data is part of a premarket notification filed by Nuvasive, Incorporated with the FDA for Nuvasive Reline System.
| Device ID | K182974 |
| 510k Number | K182974 |
| Device Name: | NuVasive Reline System |
| Classification | Thoracolumbosacral Pedicle Screw System |
| Applicant | NuVasive, Incorporated 7475 Lusk Boulevard San Diego, CA 92121 |
| Contact | Joseph De La Rosa |
| Correspondent | Joseph De La Rosa NuVasive, Incorporated 7475 Lusk Boulevard San Diego, CA 92121 |
| Product Code | NKB |
| Subsequent Product Code | KWP |
| Subsequent Product Code | KWQ |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-10-26 |
| Decision Date | 2019-02-13 |
| Summary: | summary |