K-number	K062879
Device name	TRAVERSE OCT SPINAL FIXATION SYSTEM
Applicant	Medtronic Sofamor Danek, Inc.
Product code	MNI
Device class	Class II
Decision date	Dec 22, 2006
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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TRAVERSE OCT SPINAL FIXATION SYSTEM

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