K-number	K982180
Device name	DURAGEN DURAL GRAFT MATRIX
Applicant	Integra Lifesciences Corp.
Product code	GXQ
Device class	Class II
Decision date	Jul 6, 1999
Decision	Substantially Equivalent
Regulation	882.5910

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View the full FDA submission: accessdata.fda.gov

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DURAGEN DURAL GRAFT MATRIX

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