K-number	K033340
Device name	LEKSELL SURGIPLAN WITH IMAGEMERGE
Applicant	Elekta Instrument AB
Product code	HAW
Device class	Class II
Decision date	Feb 12, 2004
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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LEKSELL SURGIPLAN WITH IMAGEMERGE

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