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Proprietary SureScan™ MRI technology is what enables patients with the InterStim™ II or InterStim™ Micro system to get full-body* 1.5 and 3T MRI scans.
GET THE BROCHUREMRI technicians trust the SureScan™ MRI brand for its simple, convenient, and streamlined workflow.
The most common adverse events associated with sacral neuromodulation include pain at implant sites, new pain, lead migration, infection, technical or device problems, adverse change in bowel or voiding function, and undesirable stimulation or sensations. Any of these may require additional surgery or cause return of symptoms.
Built upon more than 19 years of MRI research, 10 million simulated patient scans, and more than 1.2 million unique scanning scenarios, Medtronic SureScan™ MRI systems offer uncompromised MRI access.
Patients should place the InterStim™ system in MRI mode before the MRI scan and outside of the MRI scanner room. When MRI mode is activated with the smart programmer, stimulation is turned off and the “In MRI Mode” screen appears, showing MRI scan eligibility.
View MRI guidelines in the MRI Resource Library. Search by model name, product name, or device type.
VISIT LIBRARYUnder certain conditions; see approved labeling for details. Patients with InterStim™ SureScan™ MRI Leads only.