K-number	K100884
Device name	STRYKER KNIFELIGHT
Applicant	Howmedica Osteonics Corp.
Product code	FTD
Device class	Class II
Decision date	Jun 25, 2010
Decision	Substantially Equivalent
Regulation	878.4580

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View the full FDA submission: accessdata.fda.gov

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STRYKER KNIFELIGHT

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