The purpose of this post-approval study is to confirm the safety and effectiveness of Ovatio DR and VR ICDs
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
85
implantable cardioverter defibrillator
Banner Baywood
Mesa, Arizona, United States
The percentage of patients free from complications
Time frame: 6 months
Shock effectiveness for VT/VF
Time frame: 6 months
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