K-number	K221489
Device name	Artemis Proximal Femoral Nail System
Applicant	Glw, Inc.
Product code	HSB
Device class	Class II
Decision date	Oct 27, 2022
Decision	Substantially Equivalent
Regulation	888.3020

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Source

View the full FDA submission: accessdata.fda.gov

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Artemis Proximal Femoral Nail System

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