FDA 510(k) Applications Submitted by JEFFREY JOHNSON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K060025	01/04/2006	SLIMPLICITY ANTERIOR CERVICAL PLATE SYSTEM	SPINAL USA
K090033	01/06/2009	MODIFICATION TO: PSS SYSTEM	SPINAL USA
K060132	01/18/2006	SPINAL USA CEMENT RESTRICTOR SYSTEM	SPINAL USA
K080314	02/06/2008	SPINAL USA INTERBODY FUSION DEVICE	SPINAL USA
K070922	04/02/2007	MODIFICATION TO SPINAL USA VBR SYSTEM	SPINAL USA
K081196	04/28/2008	SPINAL USA VBR SYSTEM	SPINAL USA
K071438	05/23/2007	PSS SYSTEM	SPINAL USA
K061752	06/21/2006	SPINAL USA VBR SYSTEM	SPINAL USA
K092128	07/15/2009	MODIFICATION TO: PSS SYSTEM	SPINAL USA
K092193	07/21/2009	SPINAL USA INTERBODY CAGES	SPINAL USA
K092659	08/28/2009	SPINAL USA RCS ANTERIOR LUMBAR BUTRESS PLATE SYSTEM, MODEL 22-1001-25	SPINAL USA
K083118	10/22/2008	SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE	SPINAL USA
K073240	11/16/2007	PSS SYSTEM	SPINAL USA