Healthcare Professionals

InterStim II Neurostimulator

Sacral Neuromodulation

  • Interstim II Neurostimulator

Overview

The implanted InterStim™ II system electrically stimulates the sacral nerve which is thought to normalize neural communication between the bladder and brain1 and between the bowel and brain.2

INDICATIONS

INTERSTIM THERAPY FOR URINARY CONTROL

InterStim Therapy for Urinary Control is indicated for the treatment of urinary retention and the symptoms of overactive bladder, including urinary urge incontinence and significant symptoms of urgency-frequency alone or in combination, in patients who have failed or could not tolerate more conservative treatments.

This therapy is not intended for patients with mechanical obstruction such as benign prostatic hypertrophy, cancer, or urethral stricture.

INTERSTIM THERAPY FOR BOWEL CONTROL

InterStim Therapy for Bowel Control is indicated for the treatment of chronic fecal incontinence in patients who have failed or are not candidates for more conservative treatments.

Product Details

FEATURES

The InterStim II neurostimulator was developed to offer physicians a second choice of neurostimulators and to address a wider range of patient needs. The InterStim II neurostimulator is 37% smaller by displaced volume and almost 50% lighter by weight (22 g versus 42 g) than the InterStim neurostimulator model 3023. The InterStim II neurostimulator is intended for patients who will benefit from the use of a smaller implanted device, and who experience symptom control with low to moderate neurostimulation parameters.

The InterStim II neurostimulator streamlines the implant procedure with a design that eliminates the need for the lead extension and uses fewer set screws.

  • Connects directly to the lead, eliminating need for an extension
  • Accommodates three lead sizes – 28 cm, 33 cm, and 41 cm
  • Compatible with a lead insertion indicator in the lead
  • Integrates strain relief in the header
  • Incorporates radiopaque identification of the manufacturer and neurostimulator model number
  • Allows 1-screw implantation

MRI CONDITIONALLY SAFE

InterStim II model 3058 has FDA-approved labeling for 1.5 Tesla MRI head scans.

Refer to the MRI Guidelines for a complete list of conditions and instructions for use (available on the Medtronic Manuals Library).

ACCESS MRI RESOURCES

COMPATIBLE PRODUCTS

  • Tined lead model 3889 and model 3093
  • N'VisionTM clinician programmer
  • InterStim iConTM patient programmer

MANUALS AND TECHNICAL GUIDES

Access prescriber, implant, MRI, and other manuals on the Medtronic Manual Library. Search by the product name (InterStim) or model number (3058). You may also call 800-961-9055 for a copy of a manual.

MODEL SPECIFICATIONS

Model3058
Battery TypePrimary Cell
Weight22 g (0.77 oz)
Height44 mm (1.7 in)
Length51 mm (2.0 in)
*

While the precise mechanism of action of SNM has not been fully established, efficacy has been proven in clinical studies.

1

Johnson M. Transcutaneous electrical nerve stimulation (TENS). Published online Oct 15, 2012.

2

Patton V, Wiklendt L, Arkwright JW, Lubowski DZ, Dinning PG. The effect of sacral nerve stimulation on distal colonic motility in patients with fecal incontinence. Br J Surg. 2013;100:959–968.