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We continue to advance sacral neuromodulation by offering updated full-body MRI labeling.* We have improved:
New and improved MRI labeling for the InterStim™ systems with Surescan™ MRI leads.
LEARN MORE ABOUT MRIThe InterStim™ basic evaluation allows patients to explore the therapy before making a long-term decision. Test with the best and expect actionable results within a week.
FIND OUT MOREThe recharge-free InterStim™ II system may be the best choice for most people because it’s simple, convenient, and low maintenance.
The InterStim™ Micro system is the smallest sacral neuromodulation device on the market.
GET DETAILSInterStim™ II System | InterStim™ Micro System | |
---|---|---|
MRI SCANS |
Allows full-body scans* |
Allows full-body scans* |
BATTERY |
Recharge-free |
Rechargeable Overdrive™ battery technology |
BATTERY LIFE |
Approximately 5-6 years† |
At least 15 years |
DEVICE SIZE |
12.5 cm3 |
2.8 cm3 |
ROUTINE MAINTENANCE |
None |
Weekly recharging of 20 minutes‡ |
COMPONENTS/ACCESSORIES |
Smart programmer, communicator |
Smart programmer, communicator, recharger, charging dock, recharging belt |
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FIND TOOLSMedtronic provides the innovative technology, expert support, and specialized services your practice needs to thrive.
VIEW MARKETING RESOURCESThe most common adverse events experienced 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.
Complications can occur with the evaluation, including tissue damage, infection, and technical problems with the device. Patients should be instructed on operating the programmer and given precautions related to the evaluation.
Under certain conditions. See approved labeling for details. Patients with InterStim™ SureScan™ MRI leads only.
Battery life may vary based on therapy settings.
Under standard therapy settings and appropriate recharger placement.
MRI Guidelines for InterStim™ systems 97810 3058 3023 – Instructions for use (M980291A016 Rev A)