FDA 510(k) Applications Submitted by Jane Metcalf

FDA 510(k) Number	Submission Date	Device Name	Applicant
K160464	02/19/2016	Opticage(R) Expandable Interbody Fusion Device	INTERVENTIONAL SPINE, INC.
K140716	03/21/2014	OPTICAGE EXPANDABLE INTERBODY FUSION DEVICE	INTERVENTIONAL SPINE, INC.
K141313	05/20/2014	REVERSE MEDICAL MICRO VASCULAR PLUG SYSTEM	REVERSE MEDICAL CORPORATION
K152156	08/03/2015	Opticage Expandable Interbody Fusion Device	INTERVENTIONAL SPINE, INC.
K132479	08/08/2013	OPTICAGE INTERBODY FUSION DEVICE, MODEL 9080-00	INTERVENTIONAL SPINE, INC.
K182211	08/15/2018	Aurora Surgiscope System	Rebound Therapeutics Corporation
K133583	11/21/2013	OPTICAGE INTERBODY FUSION DEVICE, MODEL SERIES 9070	INTERVENTIONAL SPINE, INC.
K113527	11/30/2011	OPTICAGE INTERBODY FUSION DEVICE	INTERVENTIONAL SPINE, INC.