FDA 510(k) Applications Submitted by Martin A Yahiro

FDA 510(k) Number	Submission Date	Device Name	Applicant
K150362	02/12/2015	NuVasive CoRoent Small Interbody System	NuVasive, Incorporated
K180498	02/26/2018	NuVasive Reline Fenestrated Screws, High V+ Bone Cement	NuVasive, Incorporated
K180550	03/01/2018	NuVasive Monolith Cervical Corpectomy System	NuVasive, Incorporated
K161230	05/02/2016	NuVasive Lumbar Interbody Implants	NUVASIVE, INCORPORATED
K163491	12/12/2016	NuVasive CoRoent Small Interbody System	NuVasive, Incorporated
K153782	12/31/2015	NuVasive« Lumbar Interbody Implants	NUVASIVE, INCORPORATED
K151472	06/01/2015	NuVasive CoRoent Lumbar System	NuVasive, Incorporated
K973560	09/19/1997	BONE GRAFT HARVESTER	DS MFG., INC.