K-number	K123997
Device name	TRANS1LATERAL INTERBODY FUSION SYSTEM
Applicant	Trans1, Inc.
Product code	MAX
Device class	Class II
Decision date	Apr 1, 2013
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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TRANS1LATERAL INTERBODY FUSION SYSTEM

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