FDA 510(k) Applications Submitted by Kathleen Wong

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180431	02/16/2018	Cortina [MAX] Lumbar Cage System	NeuroStructures, Inc.
K171112	04/14/2017	Trifore(tm) Cervical Plating System	NeuroStructures, Inc.
K181590	06/18/2018	Neurostructures Cavetto« [MAX] Cervical Cage System	NeuroStructures, Inc.
K171914	06/26/2017	CortinaÖ Lumbar Cage System	NeuroStructures, Inc.
K172320	08/01/2017	Neurostructures Cavetto« Cervical Cage System	NeuroStructures, Inc.
K182195	08/14/2018	ArcoÖ-SA Lumbar Cage System	NeuroStructures, Inc.
K173077	09/29/2017	Cavetto-SA Cervical Cage System	NeuroStructures, Inc.
K173082	09/29/2017	ArcoÖ-SA Lumbar Cage System	NeuroStructures, Inc.