K-number	K202190
Device name	Oculus-SA Lumbar Cage System
Applicant	Neurostructures
Product code	OVD
Device class	Class II
Decision date	Oct 2, 2020
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Oculus-SA Lumbar Cage System

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