K-number	K220523
Device name	restor3d TiDAL Lumbar Interbody Fusion Device
Applicant	Restor3D
Product code	MAX
Device class	Class II
Decision date	Jun 17, 2022
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 Device

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