K-number	K062640
Device name	STRYKER NAVIGATION SYSTEM - CRANIAL MODULE, MODEL 6000-650-000
Applicant	Stryker Instruments
Product code	HAW
Device class	Class II
Decision date	Dec 14, 2006
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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STRYKER NAVIGATION SYSTEM - CRANIAL MODULE, MODEL 6000-650-000

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