B
BigManP
We are a manufacturer of orthopedic devices with a line of titanium implants. Over the last several years, the FDA's and EU's stance on MR compatibility has been evolving and we are getting increased pressure to address this issue in our labeling. We are planning on doing some testing to establish the MR Conditional parameters, but my question is whether 1.5 Tesla or 3 Tesla should be evaluated. What is the industry standard for this?
Thanks a lot for any insight that you can provide.
Paul
Thanks a lot for any insight that you can provide.
Paul