FDA 510(k) Applications Submitted by Michelle Cheung
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K160051 |
01/11/2016 |
NuVasive« Interfixated Interbody System |
NuVasive, Incorporated |
K180198 |
01/24/2018 |
NuVasive« VuePoint« II OCT System |
NuVasive, Incorporated |
K160916 |
04/01/2016 |
CoRoent« Ti-C System |
NUVASIVE, INCORPORATED |
K200953 |
04/09/2020 |
NuVasive« Cohere« Thoracolumbar Interbody System |
NuVasive, Incorporated |
K191553 |
06/12/2019 |
NuVaisve« Reline« Cervical System |
NuVasive, Incorporated |
K142050 |
07/28/2014 |
NUVASIVE COROENT SMALL CONTOURED INTERBODY SYSTEM |
NUVASIVE, INCORPORATED |
K162138 |
08/01/2016 |
NuVasive CoRoent Small Ti-C System |
NUVASIVE, INCORPORATED |
K173030 |
09/28/2017 |
Vertera Spine Cohere Cervical Interbody Fusion Device |
NuVasive, Incorporated |
K173153 |
09/29/2017 |
Vertera SpineÖ CoalesceÖ Thoracolumbar Interbody Fusion System |
NuVasive, Incorporated |
K143065 |
10/24/2014 |
NuVasive ALIF Buttress Plate System |
NUVASIVE, INCORPORATED |
K153419 |
11/25/2015 |
NuVasive CoRoent Thoracolumbar System |
NUVASIVE, INCORPORATED |
K193541 |
12/20/2019 |
NuVasive Cohere Thoracolumbar Interbody System |
NuVasive, Incorporated |
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