K-number	K132721
Device name	SPIWAY ENDONASAL ACCESS GUIDE
Applicant	Spiway, LLC
Product code	LYA
Device class	Class I
Decision date	Jan 29, 2014
Decision	Substantially Equivalent
Regulation	874.4780

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View the full FDA submission: accessdata.fda.gov

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SPIWAY ENDONASAL ACCESS GUIDE

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