K-number	DEN200010
Device name	Spineology Interbody Fusion System
Applicant	Spineology, Inc.
Product code	OQB
Device class	Class II
Decision date	Sep 18, 2020
Decision	Not Substantially Equivalent
Regulation	888.3085

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View the full FDA submission: accessdata.fda.gov

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Spineology Interbody Fusion System

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