K-number	K161370
Device name	Durepair Dura Regeneration Matrix
Applicant	Medtronic Neurosurgery
Product code	GXQ
Device class	Class II
Decision date	Nov 2, 2016
Decision	Substantially Equivalent
Regulation	882.5910

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Source

View the full FDA submission: accessdata.fda.gov

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Durepair Dura Regeneration Matrix

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