Medtronic Cardiac Surgery Post Market Clinical Follow-up Registry

The purpose of this registry is to provide continuing evaluation and periodic reporting of safety and clinical performance of Medtronic market-released cardiac surgery products for their intended use. Registry data will support post-market activities initiated by Medtronic and/or as directed by a government or regulatory authority.

For more information, visit: https://clinicaltrials.gov/study/NCT04073420

Inova Health Care Services                                                                   
3300 Gallows Road     
Falls Church, VA 22042

•     Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements
•     Patient has or is intended to receive or be treated with an eligible product
•     Patient within enrollment window of treatment/therapy received at the time of their initial registry enrollment, or meet criteria for retrospective enrollment.

•      Patient who is, or is expected to be inaccessible for follow up
•      Patient prohibited from participation by local law
• Patient is currently enrolled in or plans to enroll in any concurrent investigational drug and/or device study that may confound results