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FDA 510(k)

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System

K-Number: K240578 · 2024-07-31

Decision Date2024-07-31
Product CodeDTK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System is a medical device manufactured by B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2024-07-31 under approval number K240578. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System?

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System is a medical device that received FDA 510(k) clearance on 2024-07-31. It is manufactured by B.Braun Medical, Inc.. The 510(k) number is K240578.

When was VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System approved by the FDA?

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System received FDA 510(k) clearance on 2024-07-31, under approval number K240578.

What company makes VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System?

VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System is manufactured by B.Braun Medical, Inc..

What is the FDA product code for VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System?

The FDA product code for VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System is DTK.

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Official Source

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