K-number	K121253
Device name	MERIDIAN CRANIAL PERFORATOR
Applicant	Adeor Medical Technologies GmbH
Product code	HBF
Device class	Class II
Decision date	Jul 17, 2012
Decision	Substantially Equivalent
Regulation	882.4305

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Source

View the full FDA submission: accessdata.fda.gov

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MERIDIAN CRANIAL PERFORATOR

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