K-number	K150301
Device name	NavSuite3 Kit
Applicant	Stryker Leibinger GmbH & Co. KG - Navigation
Product code	HAW
Device class	Class II
Decision date	Jul 8, 2015
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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NavSuite3 Kit

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