K-number	K211837
Device name	Altus Spine Interbody Standalone Fusion System
Applicant	Altus Partners, LLC
Product code	OVD
Device class	Class II
Decision date	Apr 19, 2022
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Altus Spine Interbody Standalone Fusion System

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