Class Class II
NuVasive Modulus-C Interbody System (K223731)
Description
NuVasive Modulus-C Interbody System by Nuvasive, Inc., an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223731
Clearance Date2023-01-12
Clearance TypeSpecial
Product CodeODP
Regulation Number888.3080
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223731
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. NuVasive Modulus-C Interbody System (K223731) cites 5 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222276 | CONDUIT Cages; FIBERGRAFT BG Putty | Depuy Spine | 2022 |
| K203714 | NuVasive Thoracolumbar Interbody Systems: NuVasive CoRoent ... | Nu Vasive, Incorporated | 2021 |
| K172676 | NuVasive® Modulus-C Interbody System | Nu Vasive, Incorporated | 2017 |
| K163230 | NuVasive Modulus XLIF Interbody System | Nu Vasive, Incorporated | 2017 |
| K140003 | COROENT SMALL INTERBODY SYSTEM | Nuvasive, Inc. | 2014 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K231735 | NuVasive CoRoent Small Interbody System; NuVasive CoRoent S... | Nu Vasive, Incorporated | 2023 |
Trace the full predicate network for K223731
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.