K-number	K211935
Device name	ORIO-Ti Intervertebral Body Fusion Cage System
Applicant	Spinecraft, LLC
Product code	ODP
Device class	Class II
Decision date	Sep 30, 2021
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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ORIO-Ti Intervertebral Body Fusion Cage System

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