K-number	K061208
Device name	LIFECELL DURAL SUBSTITUTE MATRIX
Applicant	Lifecell Corp.
Product code	GXQ
Device class	Class II
Decision date	Jan 3, 2007
Decision	Substantially Equivalent
Regulation	882.5910

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View the full FDA submission: accessdata.fda.gov

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LIFECELL DURAL SUBSTITUTE MATRIX

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