Overview: The purpose of this registry is to collect information over time regarding the long term performance and use of Medtronic’s market-released products. This means that you have or will have a commercially available product that is approved for use by the US Food & Drug Administration (FDA). It is required by the FDA to monitor how Medtronic’s medical devices are working.
This trial is funded by Medtronic.
To be eligible, patients must:
Patients cannot participate if they have: