FDA 510(k) Applications Submitted by Jessica LeBlanc
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K210271 |
02/01/2021 |
NuVasive Modulus ALIF System |
NuVasive, Incorporated |
| K221751 |
06/16/2022 |
NuVasive Cohere ALIF System Intervertebral Body Fusion Device |
NuVasive, Incorporated |
| K201692 |
06/22/2020 |
NuVasive Modulus XLIF Interbody System |
NuVasive, Incorporated |
| K191974 |
07/24/2019 |
NuVasive AttraX Putty |
NuVasive, Incorporated |
| K192582 |
09/19/2019 |
NuVasive CoRoent Small Interlock System |
NuVasive, Incorporated |
| K192760 |
09/30/2019 |
NuVasive Modulus XLIF Interbody System |
NuVasive, Incorporated |
| K203253 |
11/04/2020 |
NuVasive ACP System |
NuVasive, Incorporated |
| K203714 |
12/21/2020 |
NuVasive Thoracolumbar Interbody Systems: NuVasive CoRoent Thoracolumbar System, NuVasive CoRoent XL Interfixated System, Brigade System, Brigade Lateral System, BASE Interfixated Titanium System, Coalesce Thoracolumbar Interbody Fusion System, NuVasive C |
NuVasive, Incorporated |
| K193593 |
12/23/2019 |
NuVasive 3DP Interfixated ALIF System |
NuVasive, Incorporated |
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