K-number	K234087
Device name	restor3d TIDAL Lumbar Interbody Fusion System
Applicant	Restor3D
Product code	MAX
Device class	Class II
Decision date	Jan 22, 2024
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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restor3d TIDAL Lumbar Interbody Fusion System

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