PEEK Spinal Interbody Fusion Cage

Spinal Interbody Fusion Cage

The spinal interbody fusion cage is composed of a main body and a radiopaque pin. The main body is made of PEEK material that complies with the specifications of YY/T 0660, with a grade of LT1; the radiopaque pin is made of TC4 titanium alloy material that complies with the specifications of GB/T 13810. 

Spinal Interbody Fusion Cage Indications:

1. Intervertebral disc protrusion or degeneration

2. Spondylolisthesis

3. Spinal canal stenosis

4. Cervical spondylosis

5. Spinal fracture

6. Other diseases requiring intervertebral fusion surgery

Spinal Interbody Fusion Cage Specification:

Spinal Interbody Fusion Cage Precautions:

1. This product is a single-use item and must not be reused. It is typically used in conjunction with spinal internal fixation devices;

2. This product is sterile packaged. Check the packaging for integrity before use; do not use if the packaging is damaged;

3. This product and its dedicated instruments must not be mixed with similar products from other manufacturers;

4. All products must be handled with care. Improper use or operation can lead to device damage and malfunction;

5. Remove all packaging materials before sterilization. Only sterile products and surgical instruments should be used during surgery. Once the implant comes into contact with human tissue or body fluids, it cannot be reused. After surgery, surgical instruments must be immediately cleaned and resterilized;

6. Patients must strictly follow medical advice, regularly visit the outpatient clinic within one year, and keep records;

7. For CT, MRI, and other examinations, consult the doctor's advice;

8. Used products should be disposed of in an environmentally harmless manner.