K-number	K231885
Device name	Medline UNITE® REFLEX® Nitinol Staple System
Applicant	Medline Industries, LP
Product code	JDR
Device class	Class II
Decision date	Aug 9, 2023
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Medline UNITE® REFLEX® Nitinol Staple System

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