K-number	K231923
Device name	Liberty SI Lateral Implant System
Applicant	Spinal Simplicity, LLC
Product code	OUR
Device class	Class II
Decision date	Dec 5, 2023
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Liberty SI Lateral Implant System

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