The primary objectives for the registry is to evaluate the overall incidence of serious complications or adverse events for primary implants and replacement devices, and assess the cost and time efficiency for both physicians and patients. The Registry is a multi ASC data collection registry. Data collection will occur at the time of screening, implant, and 2 weeks after implant at the time of wound check.
Study Type
OBSERVATIONAL
Enrollment
500
Cardio Surgical Partners, LLC
Lehi, Utah, United States
RECRUITINGSuccessful Implantation
Patient undergoes surgery for ICD device implantation
Time frame: Two-week follow-up assessment
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