K-number	K042391
Device name	KOLIBRI IMAGE GUIDED SURGERY SYSTEM
Applicant	Brainlab AG
Product code	HAW
Device class	Class II
Decision date	Oct 19, 2004
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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KOLIBRI IMAGE GUIDED SURGERY SYSTEM

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