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 |