Cordis earns FDA nod for Selution SLR drug-eluting balloon

Cordis earned FDA approval for its Selution SLR (sustained limus release) drug-eluting balloon (DEB) to treat coronary in-stent restenosis, the device developer announced today.

“As the first and only sirolimus drug-eluting balloon approved in the United States, Selution SLR DEB introduces a groundbreaking therapy for the treatment of coronary in-stent restenosis.” Cordis President of Americas Matt Muscari said in the announcement. “This innovative device will enable physicians to address one of the most complex coronary clinical challenges.”

Sign up for Blog Updates