Medtronic Cardiac Device Registry

Purpose of this Study

We are doing this study to learn more about the safety and performance of heart valve repair and replacement products made by Medtronic.

Who Can Participate?

Eligibility

Adults who have or will be treated with a Medtronic heart device.

What is Involved?

If you agree to be in this study we will collect information about your heart condition and surgery from your medical records.

This information will be collected before your surgery through 10 years after your surgery.

Study Details

Full Title

Medtronic Cardiac Surgery Post Market Clinical Follow-up Registry Base Protocol

Principal Investigator

Donald
Glower

Protocol Number

PRO00104466

Phase

N/A

Enrollment Status

Open to Enrollment