K-number	K072568
Device name	MODIFICATION TO OASYS SYSTEM
Applicant	Stryker Spine
Product code	KWP
Device class	Class II
Decision date	Oct 5, 2007
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO OASYS SYSTEM

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