K-number	K222415
Device name	Rexious Spinal Fixation System
Applicant	Dio Medical Corporation
Product code	NKB
Device class	Class II
Decision date	Oct 25, 2022
Decision	Substantially Equivalent
Regulation	888.3070

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Source

View the full FDA submission: accessdata.fda.gov

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Rexious Spinal Fixation System

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