K-number	K173947
Device name	Lumbar Interbody Fusion System (OLLIF)
Applicant	Advanced Research Medical, LLC
Product code	MAX
Device class	Class II
Decision date	Jul 25, 2018
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Lumbar Interbody Fusion System (OLLIF)

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