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
Dr. Steven Markowitz
Phone: (212) 746-2158
Phone: (212) 746-4857