Possibly. The participant must provide an implant card with the:

-Name of the device;
-The model and serial number of the device, or;
-Surgical report containing the information requested in #1 and #2

Once you obtain this, contact Susan Tozzi at stozzi@gmu.edu and provide information for the device safety review. You will receive an answer within two weeks on whether or not you can proceed with the MRI.