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PhysioStim™
The PhysioStim™ device provides a safe, non-invasive option for treating fractures that are difficult to heal. With an overall clinical success rate of 80 percent (up to 88 percent for fracture gaps less than 3mm), PhysioStim devices have high success rates for treating nonunion fractures. The device assists in fracture healing by delivering a pulsed electromagnetic field (PEMF) signal to the targeted fracture site.
The PhysioStim device has been approved by the FDA for the treatment of nonunion fractures. A nonunion is a fracture that has shown no visible signs of healing. 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. Typical prescribed treatment time is three hours per day. An LCD and audible alarm provide important feedback during treatment such as the operational status, treatment time remaining, battery capacity, etc.
The PhysioStim device has been approved by the FDA for the treatment of nonunion fractures. A nonunion is a fracture that has shown no visible signs of healing. 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. Typical prescribed treatment time is three hours per day. An LCD and audible alarm provide important feedback during treatment such as the operational status, treatment time remaining, battery capacity, etc.
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Key Features
- The PhysioStim device has been approved by the FDA for the treatment of nonunion fractures.
- Designed for patient ease of use.
- Works effectively when worn over clothing, casting or bracing.
- Single-piece, cordless design allows for ease of placement and patient mobility.
- The STIM onTrack™mobile app is patient-friendly and provides patients with a treatment calendar, therapy reminders, and additional educational resources.
Indications for Use
The PhysioStim device is indicated for the treatment of an established nonunion acquired secondary to trauma, excluding vertebrae and all flat bones, where the width of the nonunion defect is less than one-half the width of the bone to be treated. A nonunion is considered to be established when the fracture site shows no visibly progressive signs of healing.
Manufacturer
Orthofix
Manuf. Part No.
| Part Number | Body Application |
| 5302 | Cervical |
| 5303 | Limb |
| 5313 | Collarbone, Thigh |
| 5314R, 5314L | Shoulder - Right, Left |
| 5315 | Hip |
Manual
