K-number	K112592
Device name	AXLE PEEK INTERSPINOUS FUSION SYSTEM
Applicant	X-Spine Systems, Inc.
Product code	KWP
Device class	Class II
Decision date	Dec 5, 2011
Decision	Substantially Equivalent
Regulation	888.3050

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View the full FDA submission: accessdata.fda.gov

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AXLE PEEK INTERSPINOUS FUSION SYSTEM

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