K-number	K042034
Device name	NUVASIVE MAXCESS LIGHT GUIDE
Applicant	Nuvasive, Inc.
Product code	FST
Device class	Class II
Decision date	Oct 26, 2004
Decision	Substantially Equivalent
Regulation	878.4580

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View the full FDA submission: accessdata.fda.gov

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NUVASIVE MAXCESS LIGHT GUIDE

Everything you need for a 510(k) submission. Nothing you don't.