FDA 510(k) Applications Submitted by Michelle Willis

FDA 510(k) Number	Submission Date	Device Name	Applicant
K161081	04/18/2016	SeaSpine Shoreline ACS - Anterior Cervical Standalone System	SEASPINE ORTHOPEDICS CORPORATION
K161535	06/03/2016	SeaSpine« NewPortÖ Spinal System	SEASPINE ORTHOPEDICS CORPORATION
K150469	02/23/2015	Integra Laminoplasty System	SEASPINE, INC.
K071942	07/13/2007	MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM	MEDTRONIC SOFAMOR DANEK
K142488	09/04/2014	SeaSpine Spacer System - (Hollywood, Pacifica, Redondo, Ventura) NanoMetalene, Cambria NanoMetalene , Vu aPOD-L NanoMetalene, Vu ePOD NanoMetalene	SeaSpine, Inc.
K132859	09/12/2013	INTEGRA FACET FIXATION SYSTEM	SEASPINE, INC.