Lumbar interbody fusion cage YZRH series

transforaminalPEEKtitanium

The product is made of PEEK material (grade LT1) that meets the requirements of the YY/T0660 standard, and the developing point is made of TC4 titanium alloy material that meets the requirements of the GB/T13810 standard. It contains non-sterile packaging and radiation sterilization packaging. Sterilization period is valid for five years. Instructions The implantation of the device should be performed by a physician who fully understands the device, its use, equipment, and the required surgical techniques, and should be performed in strict accordance with the instruction manual and operation technical manual. Features X-ray transmission characteristics, elastic modulus close to human bone, with good biocompatibility. Anatomical design, wedge and arc are suitable for different endplate shapes. Metal marker for easy position of the implant. Spiny protrusions on the upper and lower surfaces, with good immediate stability. Scope of application Used in conjunction with spinal internal fixation products for orthopedic surgery to treat spinal disc herniation or degeneration, narrowing of the intervertebral space, lumbar false joints, degenerative spondylolisthesis or isthmic spondylolisthesis with unsatisfactory reduction, for cervical, lumbar, and lumbosacral Segment fusion fixation