K-number	K022579
Device name	STRYKER NAVIGATION SYSTEM-KNEE MODULE
Applicant	Stryker Leibinger
Product code	HAW
Device class	Class II
Decision date	Jun 2, 2003
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-KNEE MODULE

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