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Implantable and Fusion Device Review Form Preauthorization Phone: 800-755-1135 Preauthorization Fax: 888-247-4791 Use this form to expedite preauthorization requests for implantable and fusion devices.
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How to fill out implantable and fusion device

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How to fill out implantable and fusion device:

01
Gather all the necessary information and documentation related to the device, such as instructions for use, patient consent forms, and any applicable medical records.
02
Ensure that you have the appropriate training and qualifications to perform the procedure or assist in the filling out process. If necessary, consult with a medical professional or refer to relevant guidelines and protocols.
03
Start by carefully reviewing the instructions for use provided with the implantable and fusion device. Familiarize yourself with the device's components, indications, contraindications, warnings, and precautions.
04
Ensure that the patient's medical history and relevant diagnostic imaging are available. This information can help determine the suitability and proper placement of the device.
05
Enlist the assistance of the patient if possible. Explain the purpose of the implantable and fusion device and ensure they understand the procedure and any potential risks or complications.
06
Verify proper sterilization and aseptic techniques are followed during the filling out process to minimize the risk of infection.
07
If applicable, gather and set up any necessary tools or equipment required for the filling out procedure. This may include specialized instruments, screws, plates, or other fixation devices.
08
Follow the step-by-step instructions provided by the manufacturer for inserting and securing the implantable and fusion device. Pay close attention to proper alignment, positioning, and fixation techniques.
09
Throughout the process, maintain clear and accurate documentation of the device's insertion, placement, and any relevant measurements or adjustments made.
10
After successful filling out of the implantable and fusion device, provide appropriate post-operative care instructions to the patient. Monitor the patient's progress and address any concerns or complications that may arise.

Who needs implantable and fusion device:

01
Patients with degenerative disc diseases or spinal injuries that require stabilization or fusion of vertebrae.
02
Individuals with conditions such as herniated discs, spinal stenosis, or spondylolisthesis where surgical intervention is necessary.
03
Patients who have failed non-operative treatment options and continue to experience severe pain, nerve compression, or loss of movement due to spinal issues.
04
People with fractures or traumatic injuries to the spine that require stabilization and fusion for proper healing.
05
Individuals with deformities such as scoliosis, kyphosis, or lordosis that need correction and stabilization to prevent further progression or complications.
06
Patients with spinal tumors, infections, or other pathologies that necessitate the placement of an implantable and fusion device for support and restoration of spinal stability.
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Implantable and fusion devices are medical devices that are surgically placed inside the body to stabilize or fuse areas of the spine.
Manufacturers, importers, and device user facilities are required to file reports on implantable and fusion devices.
The required information can be filled out online on the appropriate regulatory agency's website.
The purpose of implantable and fusion devices is to provide stability and support to the spine, helping to treat conditions such as spinal fractures or deformities.
Information such as device details, adverse events, and patient outcomes must be reported on implantable and fusion devices.
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