IRB Protocol #: 1207012716

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: 

• Be greater than 18
• Have been implanted with a Medtronic device

Patients cannot participate if they have:

• Have not been implanted with a Medtronic device

NCT01524276

Medtronic Product Surveillance Registry