Device Recall Powerlink (R) System with IntuiTrak Delivery System

  • Model / Serial
    MODEL NUMBER 34-34-80L, LOTS W09-2966 AND W09-2998.
  • Product Classification
  • Device Class
    3
  • Implanted device?
    No
  • Distribution
    Recalled devices were distributed to medical centers and hospitals in OR, PA, FL, TX, MI and LA.
  • Product Description
    Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80L, LOTS W09-2966 AND W09-2998.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Endologix Inc, 11 Studebaker, Irvine CA 92618-2013
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    MODEL NUMBER 34-34-80LE, LOTS W09-2967 AND W09-3000.
  • Product Classification
  • Device Class
    3
  • Implanted device?
    No
  • Distribution
    Recalled devices were distributed to medical centers and hospitals in OR, PA, FL, TX, MI and LA.
  • Product Description
    Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80LE, LOTS W09-2967 AND W09-3000.
  • Manufacturer