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