FDA 510(k) Applications Submitted by MIKE ENSIGN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K141001	04/18/2014	ALPINE HIP STEM; ALPINE HA HIP STEM	ORTHO DEVELOPMENT
K061577	06/07/2006	OVALTWIST PEDICLE SCREW SYSTEM	SIGNUS MEDIZINTECHNIK GMBH
K092017	07/06/2009	PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)	CAPTIVA SPINE, INC
K142146	08/05/2014	IBIS PEDICLE SCREW SYSTEM	ORTHO DEVELOPMENT CORP.
K062371	08/14/2006	PREVIEW ANTERIOR CERVICAL PLATE SYSTEM	ALPHASPINE, INC.
K133386	11/05/2013	OVATION TRIBUTE HIP STEM; OVATION NARROW HIP STEM	ORTHO DEVELOPMENT CORP.
K133449	11/12/2013	KASM KNEE ARTICULATING SPACER MOLDS	ORTHO DEVELOPMENT CORP.
K073500	12/13/2007	ACTIVE ANTERIOR CERVICAL PLATE SYSTEM	SANACOR