Nu Vasive, Incorporated - FDA 510(k) Cleared Devices
112
Total
112
Cleared
0
Denied
Nu Vasive, Incorporated has 112 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.
Last cleared in 2023. Active since 2012.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Nu Vasive, Incorporated
112 devices
Cleared
Jul 11, 2023
NuVasive CoRoent Small Interbody System
Orthopedic
27d
Cleared
Jun 16, 2023
NuVasive Modulus ALIF System
Orthopedic
77d
Cleared
May 05, 2023
Rod Registration Frame
Orthopedic
29d
Cleared
Jan 11, 2023
NuVasive Reline System
Orthopedic
92d
Cleared
Oct 21, 2022
NuVasive Cohere ALIF System Intervertebral Body Fusion Device
Orthopedic
127d
Cleared
Sep 09, 2022
NuVasive Reline Cervical System
Orthopedic
119d
Cleared
Jun 21, 2022
NuVasive MOD-EX XLIF Interbody System, NuVasive MOD-EX XLIF Plated 2.0...
Orthopedic
123d
Cleared
Feb 23, 2022
NuVasive Reline Cervical System
Orthopedic
96d
Cleared
Dec 23, 2021
NuVasive Thoracolumbar Interbody Systems: NuVasive CoRoent Thoracolumbar...
Orthopedic
367d
Cleared
Nov 03, 2021
NuVasive Anterior Cervical Plate Systems
Orthopedic
90d
Cleared
Jul 29, 2021
NuVasive Pulse System
Orthopedic
153d
Cleared
May 24, 2021
NuVasive Modulus Expandable Posterior Lumbar MOD-EX PL Interbody System
Orthopedic
117d
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