K-number	K073514
Device name	TRANS1 AXIAL FIXATON SYSTEM
Applicant	Trans1 Incorporated
Product code	KWQ
Device class	Class II
Decision date	Jan 11, 2008
Decision	Substantially Equivalent
Regulation	888.3060

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View the full FDA submission: accessdata.fda.gov

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TRANS1 AXIAL FIXATON SYSTEM

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