K-number	K191367
Device name	Harrier-SA Lumbar Interbody System
Applicant	Choice Spine, LLC
Product code	MAX
Device class	Class II
Decision date	Jul 5, 2019
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Harrier-SA Lumbar Interbody System

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