Liberte MR & OTW Coronary Stent System

No FDA recalls found in the data synced 6 Oct 2026.

Trade Name

Veriflex (Liberte) Bare-Metal Coronary Stent System

Generic Name

STENT, CORONARY

PMA Number

P040016 ↗

FDA Product Code

MAF

Device Class

Class III

Advisory Committee

Cardiovascular

FDA Decision

APWD Approval withdrawn

• Niroyal Biliary Premounted Stent System

  Class II

  FDA 510(k) K012216 Active Cleared 17 Aug 2001

• Wallstent Biliary Endoprosthesis and Unistep Plus Delivery System

  Class II

  FDA 510(k) K993232 Active Cleared 30 Dec 1999

• Schneider Guidezilla Softip Guiding Catheter

  Class II

  FDA 510(k) K935292 Active Cleared 10 Jun 1994

• Wallgraft Tracheobronchial Endoprosthesis and Unistep Delivery System

  Class II

  FDA 510(k) K000001 Active Cleared 5 Jun 2000

• Walstent Tracheobronchial Endoprosthesis

  Class II

  FDA 510(k) K961507 Active Cleared 10 Jul 1996

• Wallstent Tracheobronchial Endoprosthesis

  Class II

  FDA 510(k) K961296 Active Cleared 10 Jul 1996

See all devices from Boston Scientific Scimed, Inc. →