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CervicalStim™
The CervicalStim™ device has been approved by the FDA to be worn after cervical spine fusion surgery in patients at risk for non-fusion. Please refer to the Instruction Manual for complete prescribing information.
It is a single-piece device that is lightweight, flexible and portable, allowing freedom of movement during treatment. 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, covering up to five vertebral levels. The CervicalStim device has an overall success rate of 84% in treating patients with difficult fusions.
It is a single-piece device that is lightweight, flexible and portable, allowing freedom of movement during treatment. 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, covering up to five vertebral levels. The CervicalStim device has an overall success rate of 84% in treating patients with difficult fusions.
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Key Features
- Four hour daily treatment time.
- 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
CervicalStim is a non-invasive, pulsed electromagnetic bone growth stimulator indicated as an adjunct to cervical fusion surgery in patients at high-risk for non-fusion.
Manufacturer
Orthofix
Manuf. Part No.
5505
Manual
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