K-number	K040621
Device name	ACELL UBM SURGICAL MESH
Applicant	Acell, Inc.
Product code	FTM
Device class	Class II
Decision date	Apr 14, 2004
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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ACELL UBM SURGICAL MESH

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