Ventricular Tachycardia Clinical Trial
Official title:
Abbott Ventricular Tachycardia Post Approval Study
This post-approval study (PAS) is designed to provide continued clinical evidence to confirm the long-term safety and effectiveness of the FlexAbilityTM Ablation Catheter, Sensor EnabledTM (FlexAbility SE) for the treatment of ventricular tachycardia in a post-market environment. This is a prospective, single arm, open-label, multi-center, observational study.
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Status | Clinical Trial | Phase | |
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