FDA 510(k) Applications Submitted by Moti Altarac

FDA 510(k) Number	Submission Date	Device Name	Applicant
K200115	01/21/2020	Cavetto-SA Cervical Cage System	NeuroStructures, Inc.
K200927	04/07/2020	Transept Cervical Plate System	Neurostructures, Inc.
K201769	06/29/2020	Cavetto [MAX] Cervical Cage System	NeuroStructures, Inc.
K202190	08/05/2020	Oculus-SA Lumbar Cage System	Neurostructures
K192248	08/19/2019	CortinaÖ [MAX] Lumbar Cage System	NeuroStructures, Inc.
K153097	10/26/2015	BelvedereÖ Lateral Plating System	NEUROSTRUCTURES, INC.
K143230	11/10/2014	Palladian Lumbar Pedicle Screw System	Neurostructures, Inc.