K-number	K160976
Device name	Altus Spine Interbody Fusion System
Applicant	Altus Partners, LLC
Product code	MAX
Device class	Class II
Decision date	Jan 25, 2017
Decision	Substantially Equivalent
Regulation	888.3080

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View the full FDA submission: accessdata.fda.gov

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Altus Spine Interbody Fusion System

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