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| Model Number: | Posterior Spinal Screw-rod System |
| MOQ: | 4 pieces |
| Price: | Negotiable |
| Delivery Time: | After receiving the payment, we will send the express within 7 working days |
| Payment Terms: | L/C, T/T |
Quick Detail:
| Indications | * Degenerative disc disease |
| * Spondylolisthesis | |
| * Trauma(i.e. fracture or dislocation) | |
| * Tumor | |
| * Deformities | |
| * Spinal Stenosis | |
| * Failed previous fusion | |
| * Deformity(i.e.kyphosis, lordosis and/or scoliosis) | |
| Specification |
Diameter:4.5mm～7.5mm (Interval between D is: 0.5mm ) |
| With packing weight | 10g |
| Warranty | 5 years |
| Classification | Class III |
| Material | Titanium |
| OEM | Avaliable |
| Place of Origin: | China |
| Type | Posterior Spinal Screw-rod System |
| Certification | CE / ISO13485:2016 |
| MOQ | 4 pieces |
| Price: | Negotiable |
| Packaging Details | Original packaging + carton |
| Payment Terms: | Bank transfer |
| Supply Ability: | 1,0000 pieces per month |
| Delivery Time: | After receiving the payment, we will send the express within 7 working days |
| Shipping | FEDEX or Designate |
| Product Structure and Performance |
The system is composed of pedicle screw, pedicle rod, screw plug,connector etc. The materials aretitanium alloy Ti6Al4V which meet the requirement of ISO 5832-3.The surface oftitanium productis treated by anodic oxidation coloring. The products are supplied non-sterile. |
| Type | Posterior Spinal Pedicle Screw |
| Specifications: | Monoaxial Pedicle Screw ( D:4.5mm～7.5mm L:20mm～80mm ) |
| Polyaxial Pedicle Screw ( D:4.5mm～7.5mm L:20mm～80mm ) | |
| Monoaxial Expandable Pedicle Screw ( D:4.5mm～7.5mm L:20mm～80mm ) | |
| Cement Pedicle Screw ( D:4.5mm～7.5mm L:20mm～60mm ) | |
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Screws include self tapping and non-self tapping |
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| Attentions | 1. Please carefully read the instruction before use. |
| 2. Before the surgery, determine the surgery plan according to the symptom, sign and the image check. | |
| 3. MR examination can be carried out onTi6Al4V product according to routine parameters of the hospital. | |
| 4. Choose the products and special matching tools with suitable specification and model according to the symptom and the position of patients. | |
| 5. Perform the surgery under the directions of an experienced surgeon. | |
| 6. The surgeon shall describe the relevant precautions in details to the patients before the surgery. | |
| 7. At the delivery time, if the product is found scratched, damaged, and bended or cracked, it cannot be used anymore. | |
| 8. The implants and tools provided by our company are not sterilized but the devices must be sterilized before the surgery. We recommend the method of high pressure steaming for sterilization. | |
| 9. Any activities in the early post-operation period, if being conducted improperly in method or extent, would possibly cause the invalidation of the metal implant, such as fixation loosening, broken or bending, etc. For this reason, the time, method and extent of activity in the early post-operation period shall be conducted strictly under the correct instruction of the surgeon, and shall be implemented step by step. | |
| 10. Before healing of bone grafting in early post-operation period, the external fixation shall be used for 6 to 12 weeks. | |
| 11. The product is disposable. | |
| 12. And it is forbidden to be used with products of other materials and model or from other companies. | |
| 13. To avoid contamination, this product should be disposed as infectious medical waste disposal method. | |
| Warning: |
The products and instruments should be sterilized before use.Recommended to meet the EN ISO 17665-1 related requirements of the high pressure steam sterilization method. Recommended sterilization conditions:Down-draining steam sterilizer: temperature: 121℃; duration of exposure: 30 minutes; barometric pressure: 102.9kPa(1.05kg/cm2);drying time:45 minutes.High pressure steam sterilizer must be approved by the hospital and inspection regularly to ensure the medical device can reach the recommended sterilization temperature during the exposure period. |
| The product is disposable and should not be reused under any circumstances.Used implants may contain many acquired flaws, or the integrity of itself may be damaged, which will shorten the service life or cause cross infection. Whether the appearance of used implants is good or not, it's strictly prohibited to be reused. Installation and Operating Instructions |
6.0mm Spinal Screws-Rod System:
Using zero-angle thread technology, it can effectively prevent the nail arm from expanding.
Adopt 14mm outer diameter thickened nail arm, the nail arm strength is higher.
Deeper thread profile, stronger pullout resistance.
The traditional ball head structure has higher anti-spin ability, and the ball head is not easy to fall out and damage.
Cassette cross connector is more stable and has lower notch than traditional horizontal connector.
Product Specifications
