K-number	K052211
Device name	DUREPAIR DURA REGENERATION MATRIX
Applicant	Medtronic Neurosurgery
Product code	GXQ
Device class	Class II
Decision date	Sep 14, 2005
Decision	Substantially Equivalent
Regulation	882.5910

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View the full FDA submission: accessdata.fda.gov

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DUREPAIR DURA REGENERATION MATRIX

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