K-number	K210425
Device name	Catalyft PL Expandable Interbody System
Applicant	Medtronic Sofamor Danek USA, Inc.
Product code	MAX
Device class	Class II
Decision date	May 24, 2021
Decision	Substantially Equivalent
Regulation	888.3080

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Source

View the full FDA submission: accessdata.fda.gov

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Catalyft PL Expandable Interbody System

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