K-number	K122456
Device name	MRII CRAINIAL DRILL
Applicant	Mri Interventions, Inc.
Product code	HBG
Device class	Class II
Decision date	Mar 22, 2013
Decision	Substantially Equivalent
Regulation	882.4300

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View the full FDA submission: accessdata.fda.gov

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MRII CRAINIAL DRILL

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