K-number	K101765
Device name	KYPHON ANCHOR FACET SCREW SYSTEM
Applicant	Medtronic Spine, LLC
Product code	MRW
Device class	Class U
Decision date	Oct 22, 2010
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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KYPHON ANCHOR FACET SCREW SYSTEM

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