K-number	K231836
Device name	ClariVy Cervical IBF System
Applicant	Vy Spine, LLC
Product code	ODP
Device class	Class II
Decision date	Oct 30, 2023
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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ClariVy Cervical IBF System

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ClariVy Cervical IBF System