K-number	K081377
Device name	NUVASIVE SURGICAL MESH SYSTEM
Applicant	Nuvasive, Inc.
Product code	FTL
Device class	Class II
Decision date	Jan 15, 2009
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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NUVASIVE SURGICAL MESH SYSTEM

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