K-number	K002334
Device name	MACROPORENS CRANILOC
Applicant	Macropore Biosurgery, Inc.
Product code	GXR
Device class	Class II
Decision date	May 2, 2001
Decision	Substantially Equivalent
Regulation	882.5250

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View the full FDA submission: accessdata.fda.gov

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MACROPORENS CRANILOC

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