K-number	K171938
Device name	KYPHON Xpede Bone Cement, CD HORIZON Fenestrated Screw Set
Applicant	Medtronic
Product code	PML
Device class	Class II
Decision date	Oct 23, 2017
Decision	Substantially Equivalent
Regulation	888.3027

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Source

View the full FDA submission: accessdata.fda.gov

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KYPHON Xpede Bone Cement, CD HORIZON Fenestrated Screw Set

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