FDA 510(k) Applications Submitted by John McIntyre

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140178	01/24/2014	ELLIPSE MAGEC SPINAL BRACING AND DISTRACTION SYSTEM	ELLIPSE TECHNOLOGIES, INC.
K140613	03/10/2014	MAGEC SPINAL BRACING AND DISTRACTION SYSTEM	ELLIPSE TECHNOLOGIES INC.
K141278	05/16/2014	MAGEC SPINAL BRACING AND DISTRACTION SYSTEM	ELLIPSE TECHNOLOGIES, INC.
K131490	05/23/2013	ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM	ELLIPSE TECHNOLOGIES, INC.
K131677	06/10/2013	PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM	ELLIPSE TECHNOLOGIES INC.
K101997	07/15/2010	ELLIPSE INTRAMEDULLARY LIMB LENGTHENING SYSTEM	ELLIPSE TECHNOLOGIES, INC.
K152370	08/21/2015	PRECICE Trauma Nail System	Ellipse Technologies Incorporated
K133289	10/25/2013	PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM	ELLIPSE TECHNOLOGIES, INC.