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Nu Vasive, Incorporated

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
112
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231735NuVasive CoRoent Small Interbody System; NuVasive CoRoent Small Contoured Interbody System; NuVasiveJuly 11, 2023
K230894NuVasive Modulus ALIF SystemJune 16, 2023
K230989Rod Registration FrameMay 5, 2023
K223181NuVasive Reline SystemJanuary 11, 2023
K221751NuVasive Cohere ALIF System Intervertebral Body Fusion DeviceOctober 21, 2022
K221388NuVasive Reline Cervical SystemSeptember 9, 2022
K220478NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2.0 Interbody SystemJune 21, 2022
K213654NuVasive Reline Cervical SystemFebruary 23, 2022
K203714NuVasive Thoracolumbar Interbody Systems: NuVasive CoRoent Thoracolumbar System, NuVasive CoRoent XLDecember 23, 2021
K212446NuVasive Anterior Cervical Plate SystemsNovember 3, 2021
K210574NuVasive Pulse SystemJuly 29, 2021
K210214NuVasive Modulus Expandable Posterior Lumbar MOD-EX PL Interbody SystemMay 24, 2021
K210439NuVasive MOD-EX XLIF Interbody SystemMay 12, 2021
K210271NuVasive Modulus ALIF SystemMarch 1, 2021
K203201NuVasive Thoracolumbar Interbody Systems: CoRoent Thoracolumbar System, CoRoent XL Interfixated SystJanuary 12, 2021
K203253NuVasive ACP SystemDecember 3, 2020
K200719NuVasive Navigation.S InstrumentsDecember 2, 2020
K201692NuVasive Modulus XLIF Interbody SystemOctober 29, 2020
K200953NuVasive® Cohere® Thoracolumbar Interbody SystemOctober 6, 2020
K201820NuVasive Thoracolumbar Interbody Systems: CoRoent Thoracolumbar System, CoRoent XL Interfixated SystSeptember 25, 2020