K-number	K180556
Device name	Corelink Foundation 3D Anterior Lumbar System
Applicant	Corelink, LLC
Product code	MAX
Device class	Class II
Decision date	Jul 27, 2018
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Corelink Foundation 3D Anterior Lumbar System

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