K-number	K163409
Device name	Rampart(TM) T Lumbar Interbody Fusion Device
Applicant	Spineology, Inc.
Product code	MAX
Device class	Class II
Decision date	Mar 8, 2017
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Rampart(TM) T Lumbar Interbody Fusion Device

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