K-number	K233513
Device name	Remex Spine Surgery Navigation System II
Applicant	Remex Medical Corp.
Product code	OLO
Device class	Class II
Decision date	May 1, 2024
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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Remex Spine Surgery Navigation System II

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