K-number	K991706
Device name	VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE
Applicant	Stryker Corp.
Product code	HAW
Device class	Class II
Decision date	Dec 7, 1999
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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VIRTUOSO-STEREOTAXIC PLANNING SOFTWARE

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