K-number	K150825
Device name	Collagen Dural Regeneration Matrix
Applicant	Collagen Matrix, Inc.
Product code	GXQ
Device class	Class II
Decision date	Nov 20, 2015
Decision	Substantially Equivalent
Regulation	882.5910

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View the full FDA submission: accessdata.fda.gov

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Collagen Dural Regeneration Matrix

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