K-number	K080250
Device name	LEKSELL SURGIPLAN, MODEL 1006947
Applicant	Elekta Instrument AB
Product code	HAW
Device class	Class II
Decision date	May 13, 2008
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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LEKSELL SURGIPLAN, MODEL 1006947

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