MD+DI Online is part of the Informa Markets Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

10 Hot Devices We Can't Get in the U.S.—Endologix's Nellix

10 Hot Devices We Can't Get in the U.S.—Endologix's Nellix
 

Endologix's Nellix

Endologix developed the Nellix endovascular aneurysm sealing system to give a minimally invasive option to patients who cannot receive conventional endovascular aneurysm repair (EVAR) for abdominal aortic aneurysms (AAAs). These patients may have challenging aortic anatomy that does not fit traditional EVAR devices. 

The Nellix system uses polymer-filled endobags to seal off the aortic aneurysm and prevent further aneurysm expansion or rupture.

Nellix received CE Mark in January 2013 and has been much buzzed about at vascular medical meetings ever since. Analysts expect Nellix to gain FDA approval near the end of 2016. 

             

[Image courtesy of ENDOLOGIX, INC.]  

Hide comments
account-default-image

Comments

  • Allowed HTML tags: <em> <strong> <blockquote> <br> <p>

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.
Publish