Spinal Internal Fixation Series
Following lumbar discectomy, interbody fusion and fixation can be achieved by implanting a spinal cage, which is applicable to procedures such as PLIF, TLIF, and MIS-TLIF.
Please contact your local distributor for more information.
-
Optimized bullet-shaped design for easy implantation; three tantalum radiopaque markers for clear fluoroscopic visualization of the fusion cage position. -
The dental-shaped protrusions prevent implant dislodgement, thereby achieving initial implant stability. The rounded-edge shield design of the dental-shaped protrusions mitigates stress concentration during contact between the fusion cage and the endplates, thus reducing the risk of postoperative endplate fracture. The extra-large bone-grafting window increases the volume of bone graft, enhances the contact area with the superior and inferior endplates, and improves the fusion rate. -

Curved support surface
It conforms closely to the superior and inferior endplates, better matching the human anatomical structure and promoting fusion. -
The tail-edge chamfer design prevents postoperative irritation of the dural sac. A tapping device is added to the distal end of the implantation tool to avoid applying excessive force to the connecting screw, thereby preventing loosening or even thread damage. The chamfered connection hole at the tail end facilitates secondary installation of the implant during intraoperative adjustments. Made from PEEK, this material exhibits excellent biocompatibility, a modulus of elasticity close to that of bone, and no stress shielding, thus enhancing fusion rates.

Indications
-
For patients requiring segmental fusion of the lumbar and lumbosacral segments.
-
Patients with degenerative disc disease and spinal instability
-
Patients with vertebral slippage
-
Patients undergoing revision surgery after simple discectomy
-
Patients with pseudoarthrosis or failed lumbar spinal fusion
Contraindication
-
Tumor patients with bone destruction
-
Patients with severe osteoporosis
-
Patients with severe unstable burst fractures or compression fractures
-
Patients in the acute infection phase
-
Patients with extensive epidural scar formation
Please contact your local distributor for more information.