K-number	K131156
Device name	LANX SPINAL FIXATION SYSTEM
Applicant	Lanx, Inc.
Product code	KWP
Device class	Class II
Decision date	May 24, 2013
Decision	Substantially Equivalent
Regulation	888.3050

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Source

View the full FDA submission: accessdata.fda.gov

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LANX SPINAL FIXATION SYSTEM

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