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SpinalStim™
SpinalStim™
SpinalStim™
SpinalStim™
SpinalStim™
SpinalStim™
SpinalStim™
SpinalStim™

SpinalStim™

The SpinalStim™ device is FDA approved to be used after spinal fusion surgery or to be used to treat a failed fusion from a previous surgery. For complete prescribing information, please refer to the Instruction Manual.

This single-piece device is lightweight, flexible and portable, allowing freedom of movement during treatment. The typical prescribed treatment time is two hours per day. An LCD and audible alarm provide important feedback during treatment such as the operational status, treatment time remaining, battery capacity, etc.

This device utilizes Orthofix PEMF technology that provides 360 degrees of treatment coverage around the fusion site. The SpinalStim device has an overall success rate of 92% in treating spinal fusion surgery patients. In addition, the SpinalStim device can be used for treatment of a failed spinal fusion, reducing the need for a revision surgery.
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Key Features
  • Works effectively when worn over clothing or bracing.
  • Cordless design enables you to keep moving while healing.
  • A patient friendly mobile app, STIM onTrack™, with patient usage data.
  • Daily treatment reminder via the STIM onTrack™ mobile app.
Indications for Use
SpinalStim is a noninvasive electromagnetic bone growth stimulator indicated as a spinal fusion adjunct to increase the probability of fusion success and as a nonoperative treatment of salvage of failed spinal fusion, where a minimum of nine months has elapsed since the last surgery.
Manufacturer
Orthofix
Manuf. Part No.
5212
Manual
Orthofix spinalstim manual
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