K-number	K223412
Device name	LumiVy Lumbar IBF System
Applicant	Vy Spine, LLC
Product code	MAX
Device class	Class II
Decision date	Jan 6, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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LumiVy Lumbar IBF System

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LumiVy Lumbar IBF System