FDA 510(k) Applications Submitted by PETER LOWENDAHL

FDA 510(k) Number	Submission Date	Device Name	Applicant
K080250	01/31/2008	LEKSELL SURGIPLAN, MODEL 1006947	ELEKTA INSTRUMENT AB
K080355	02/11/2008	LEKSELL STEREOTACTIC SYSTEM WITH REUSABLE FIXATION SCREWS	ELEKTA INSTRUMENT AB
K051022	04/22/2005	GAMMAPLAN	ELEKTA INSTRUMENT AB
K031980	06/26/2003	MODIFICATION TO LEKSELL STEREOTACTIC SYSTEM	ELEKTA INSTRUMENT AB
K031999	06/27/2003	ELEKTA LEKSELL STEREOTACTIC SYSTEM WITH MR POST KIT	ELEKTA INSTRUMENT AB
K051746	06/29/2005	ELEKTA ESARTE FRAME SYSTEM	ELEKTA INSTRUMENT AB
K061941	07/10/2006	LEKSELL GAMMA KNIFE PERFEXION, MODEL 715000	ELEKTA INSTRUMENT AB
K033340	10/17/2003	LEKSELL SURGIPLAN WITH IMAGEMERGE	ELEKTA INSTRUMENT AB