K-number	K060506
Device name	STRYKER SPINE VLIFT VERTEBRAL BODY REPLACEMENT SYSTEM
Applicant	Stryker Spine
Product code	MQP
Device class	Class II
Decision date	May 25, 2006
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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STRYKER SPINE VLIFT VERTEBRAL BODY REPLACEMENT SYSTEM

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