K-number	K002509
Device name	NOVALIS (SHAPED BEAM SURGERY SYSTEM)
Applicant	Brainlab AG
Product code	MUJ
Device class	Class II
Decision date	Nov 3, 2000
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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NOVALIS (SHAPED BEAM SURGERY SYSTEM)

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