Medtronic Endovascular Innovations
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- Devices
- 1
What Medtronic Endovascular Innovations makes
Medtronic Endovascular Innovations manufactures the RELIANT stent graft balloon catheter, a device used for endovascular aneurysm repair to treat abdominal aortic aneurysms by positioning and expanding stent grafts within the aorta.
The RELIANT stent graft balloon catheter is classified as a Class II medical device in the US and is listed under FDA’s 510(k) clearance process. The company is based in the United States.
Catalogue
Reliant Stent Graft Balloon Catheter Ref K050038
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medtronic Endovascular Innovations have in the registry?
The registry currently lists 1 device for Medtronic Endovascular Innovations. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtronic Endovascular Innovations's devices?
Among its 1 most recently registered device, Medtronic Endovascular Innovations has devices listed in FDA 510(k) (1 device).
What risk classes do Medtronic Endovascular Innovations's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medtronic Endovascular Innovations's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medtronic Endovascular Innovations in the registry?
The most recently registered devices listed for Medtronic Endovascular Innovations include RELIANT STENT GRAFT BALLOON CATHETER.