K-number	K230219
Device name	Eminent Spine 3D Lumbar Interbody Fusion Systems
Applicant	Eminent Spine, LLC
Product code	MAX
Device class	Class II
Decision date	May 16, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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Eminent Spine 3D Lumbar Interbody Fusion Systems

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