K-number	K193000
Device name	Hexanium® ACIF
Applicant	Spinevision, S.A.S.
Product code	OVE
Device class	Class II
Decision date	Oct 20, 2020
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Hexanium® ACIF

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