Longitudinal Surveillance Study of the 4-SITE Lead/Header System

The objective of the LSS of 4-SITE Study is to prospectively determine the chronic
complication-free rate of the 4-SITE Lead/Header System in order to verify its clinical
performance, long-term reliability and functional integrity. The LSS of 4-SITE Study is a
non-randomized, multi-center, global clinical investigation of subjects implanted with the
4-SITE Lead/Header System. The study is designed to collect product performance information,
any reportable adverse events and withdrawal data.

The primary purpose of this study is to evaluate, document and report on the appropriate
clinical performance, the long-term reliability and the functional integrity of the 4-SITE
Lead/Header System. This 4-SITE Lead/Header System consists of a 4-SITE ENDOTAK® RELIANCE
defibrillation lead connected to a 4-SITE Header (which is the only PG component under study)
of a single or dual chamber (VR and DR) implantable cardioverter defibrillator (ICD) or a
cardiac resynchronization therapy ICD (CRT-D) BSC pulse generator. Additionally,
system-related diagnostic information and implant data will be collected during the conduct
of this study.

Inclusion Criteria:

- medically indicated for ICD/CRT-D

- received/plan to receive study lead

- willing for long-term follow-up

Exclusion Criteria:

- unwilling to comply with protocol