Your best choice for sacral neuromodulation.
Choose the best InterStim™ system for each patient. Both systems are full-body* MRI eligible and deliver the same therapy with long-term relief.
The most common adverse events experienced during clinical studies 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.
Under certain conditions; see approved labeling for details. Patients with InterStim™ SureScan™ MRI Leads only.