K-number	K210090
Device name	Impulse AM Interbody Fusion System
Applicant	Degen Medical
Product code	MAX
Device class	Class II
Decision date	Aug 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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Impulse AM Interbody Fusion System

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