K-number	K071877
Device name	LANX SPINAL FIXATION SYSTEM
Applicant	Lanx, LLC
Product code	MNI
Device class	Class II
Decision date	Sep 17, 2007
Decision	Substantially Equivalent
Regulation	888.3070

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View the full FDA submission: accessdata.fda.gov

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LANX SPINAL FIXATION SYSTEM

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