For patients recovering from
The CervicalStim™device has been approved by the FDA to be worn after cervical spine fusion surgery in patients at risk for non-fusion.6, 13 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.
Designed for patient ease of use
This device utilizes Orthofix PEMF technology that provides 360 degrees of treatment coverage around the fusion site, covering up to five vertebral levels.18 The CervicalStim device has an overall success rate of 84% in treating patients with difficult fusions.6, 13
Why do physicians prescribe a CervicalStim device?
* STIM onTrack mobile app is available as an accessory for US model devices only