FDA 510(k) Applications Submitted by NUVASIVE INCORPORATED

FDA 510(k) Number	Submission Date	Device Name	Applicant
K193506	12/18/2019	NuVasive X-Core Expandable VBR System, NuVasive X-Core Mini Cervical Expandable VBR System	NuVasive Incorporated
K161442	05/25/2016	NuVasive« CoRoent« Small InterlockÖ System	NUVASIVE INCORPORATED
K152943	10/05/2015	NuVasive Foundation-LL System	NUVASIVE INCORPORATED
K163230	11/17/2016	NuVasive Modulus XLIF Interbody System	NUVASIVE INCORPORATED
K153627	12/18/2015	NuVasive« TLX Interbody System	NUVASIVE INCORPORATED
K162313	08/18/2016	NuVasive Next Generation NVM5 System	NUVASIVE INCORPORATED
K152942	10/05/2015	NuVasiveNVM5 System	NUVASIVE INCORPORATED
K143684	12/24/2014	NuVasive Reline System	NUVASIVE INCORPORATED