K-number	K200958
Device name	MODULIF-A Anterior Lumbar Interbody Fusion System
Applicant	Spinal Stability, LLC
Product code	MAX
Device class	Class II
Decision date	Aug 28, 2020
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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MODULIF-A Anterior Lumbar Interbody Fusion System

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