K-number	K181589
Device name	Curiteva Lumbar Interbody Fusion System
Applicant	Curiteva, LLC
Product code	MAX
Device class	Class II
Decision date	Dec 20, 2018
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Curiteva Lumbar Interbody Fusion System

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