Express LD Iliac Premounted Stent System

FDA premarket approval P090003 · Stent, Iliac

PMA numberP090003

Approval

Applicant
Boston Scientific Corporation
Received
February 23, 2009
Decision date
March 5, 2010 (APPR)
Supplements
53, latest May 6, 2026
Product code
NIO – Stent, Iliac

Official FDA PMA record

Approval order statement

APPROVAL FOR THE EXPRESS LD ILIAC PREMOUNTED STENT SYSTEM. THE DEVICE IS INDICATED FOR THE TREATMENT OF ATHEROSCLEROTIC LESIONS FOUND IN ILIAC ARTERIES UP TO 100 MM IN LENGTH, WITH A REFERENCE DIAMETER OF 6 MM TO 10 MM.