Safety and Performance Study of the Siello S Pacing Lead

TERMINATED

Status

1758

Enrollment

INDUSTRY

Sponsor class

Stopped On April 15, 2019, BIOTRONIK received FDA approval to transition the ongoing SIELLO Post Approval Registry to a new EP PASSION real-world data methodology.

Conditions

Safety and Effectiveness of the Siello S Lead

Interventions

DEVICE: market-released BIOTRONIK pacemaker system including one or two Siello S leads.

Sponsor

Biotronik, Inc.