prmarks logo

Xeltis announces FDA Breakthrough Device Designation for aXessTM and first patient treated in US pivotal trial

News provide by
702Padmin
Nov 14, 2024, 0:30 AM PST

Share this article

Designation recognizes aXess has the potential of providing a more effective vascular access option for dialysis patients, bringing significant advantages over current therapies First patient treated in US pivotal trial, marking significant clinical milestone EINDHOVEN, The Netherlands,…