K-number	K183049
Device name	Reliance Lumbar IBF System
Applicant	Reliance Medical Systems, LLC
Product code	MAX
Device class	Class II
Decision date	Feb 15, 2019
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Reliance Lumbar IBF System

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