K-number	K241468
Device name	Vertiwedge® Intraosseous System
Applicant	Foundation Surgical Group, Inc.
Product code	MQP
Device class	Class II
Decision date	Nov 7, 2024
Decision	Substantially Equivalent
Regulation	888.3060

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Source

View the full FDA submission: accessdata.fda.gov

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Vertiwedge® Intraosseous System

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