Product Surveillance Registry (PRS) 

Principal Investigator:  Rudolph Evonich, III, MD

  • Study involving collecting information about the cardiac leads and the device you have already received
  • No experimental procedures or devices are involved in this study.
  • The devices involved in this study are approved by the Food & Drug Administration (FDA) and are used here regularly. 
  • Medtronic or other manufacturer’s make these devices and Medtronic makes the leads attached to the devices. 
  • The information collected in the study is used to evaluate the devices and leads and is crucial for providing early notification about potential lead performance problems and their management.