K-number	K081635
Device name	INTEGRA MESHED BILAYER WOUND MATRIX
Applicant	Integra Lifesciences Corp.
Product code	KGN
Device class	Class U
Decision date	Dec 4, 2008
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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INTEGRA MESHED BILAYER WOUND MATRIX

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