K-number	K160663
Device name	Lumbar Interbody Fusion System (ALIF, PLIF, LLIF, TPLIF)
Applicant	Evolution Spine, LLC
Product code	MAX
Device class	Class II
Decision date	Nov 16, 2016
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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Lumbar Interbody Fusion System (ALIF, PLIF, LLIF, TPLIF)

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