Vertiwedge® Intraosseous System
K-Number: K241468 · 2024-11-07
ApplicantFoundation Surgical Group, Inc.
Decision Date2024-11-07
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Vertiwedge® Intraosseous System is a medical device manufactured by Foundation Surgical Group, Inc.. It received FDA 510(k) clearance on 2024-11-07 under approval number K241468. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vertiwedge® Intraosseous System?
Vertiwedge® Intraosseous System is a medical device that received FDA 510(k) clearance on 2024-11-07. It is manufactured by Foundation Surgical Group, Inc.. The 510(k) number is K241468.
When was Vertiwedge® Intraosseous System approved by the FDA?
Vertiwedge® Intraosseous System received FDA 510(k) clearance on 2024-11-07, under approval number K241468.
What company makes Vertiwedge® Intraosseous System?
Vertiwedge® Intraosseous System is manufactured by Foundation Surgical Group, Inc..
What is the FDA product code for Vertiwedge® Intraosseous System?
The FDA product code for Vertiwedge® Intraosseous System is MQP.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.