nEw3 Post-approval Study

Update Il y a 4 ans
Reference: NCT01076374

Woman and Man

Extract

The primary purpose of this study is to assess the long term reliability of the Medtronic Adapta®/Sensia™/Versa™ platform of devices. This study is required by FDA as a condition of approval of nEw3 devices. Patients will be followed for 5 years after implant. This study utilizes data collected from the System Longevity Study (SLS).


Inclusion criteria

  • Arrhythmia ,Bradycardia


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