Endovascular suturing system

FDA product code OTD · Class 2 · 18 devices · 255 reports · 27 deaths reported · 2 devices named in recalls

• Heli-FX™ EndoAnchor™ System SA-85

  Medtronic, Inc. · Endovascular suturing system
  6 deaths70 reports
• Heli-FX™ EndoAnchor™ System HG-18-90-22

  Medtronic, Inc. · Endovascular suturing system
  1 recall1 report
• APTUS Heli-FX® SA-85

  Medtronic, Inc. · Endovascular suturing system
  8 deaths50 reports
• Heli-FX™ EndoAnchor™ System HG-18-90-42

  Medtronic, Inc. · Endovascular suturing system
  1 recall0 reports
• Heli-FX™ EndoAnchor™ System SA-85

  Medtronic, Inc. · Endovascular suturing system
  4 deaths44 reports
• Heli-FX™ EndoAnchor™ System SA-85

  Medtronic, Inc. · Endovascular suturing system
  6 deaths41 reports
• Heli-FX™ EndoAnchor™ System SG-64

  Medtronic, Inc. · Endovascular suturing system
  18 reports
• APTUS Heli-FX® HG-16-62-28

  Medtronic Vascular, Inc. · Endovascular suturing system
  6 reports
• Heli-FX™ EndoAnchor™ System HG-16-62-28

  Medtronic, Inc. · Endovascular suturing system
  5 reports
• Heli-FX™ EndoAnchor™ System HA-18-114

  Medtronic, Inc. · Endovascular suturing system
  1 death4 reports
• Heli-FX™ EndoAnchor™ System HA-18-114

  Medtronic Vascular, Inc. · Endovascular suturing system
  4 reports
• APTUS Heli-FX® SG-64

  Medtronic, Inc. · Endovascular suturing system
  2 deaths3 reports
• Heli-FX™ EndoAnchor™ System HG-18-90-32

  Medtronic, Inc. · Endovascular suturing system
  3 reports
• Heli-FX™ EndoAnchor™ System HG-16-62-28

  Medtronic, Inc. · Endovascular suturing system
  2 reports
• APTUS Heli-FX® HA-18-114

  Medtronic Vascular, Inc. · Endovascular suturing system
  1 report
• Heli-FX™ EndoAnchor™ System SG-64

  Medtronic, Inc. · Endovascular suturing system
  1 report
• Heli-FX™ EndoAnchor™ System HG-18-90-42

  Medtronic, Inc. · Endovascular suturing system
  1 report
• Heli-FX™ EndoAnchor™ System HG-18-90-42

  Medtronic, Inc. · Endovascular suturing system
  1 report