| This year was the tenth anniversary of the establishment of Centinel Spine, but the company has been in business for more than ten years. It is understood that Centinel is made up of the merger of Raymerica and Surgicraft. Both companies are developing surgical techniques and implants. A pioneer company to ease spinal disorders. Centinel Spine is now the largest private spine company and is the leader in supporting spine technology. In addition to celebrating its tenth anniversary, Centinel has another reason to celebrate: It has received 510 (k) approval from the FDA (United States Food and Drug Administration) to sell its integrated interbody fusion cage and non-integrated intervertebral space. The FLX platform of the cage, with the FDA continuing to review and manage additive manufacturing in the manufacture of medical devices, more and more 3D medical devices have received medical approval. It is reported that, 3D printing The FLX device is made entirely of titanium and has a combination of solid and porous transmissive parts, designed to reduce mechanical stiffness and improve visibility compared to solid titanium implants. The FLX device also features a proprietary FUSE-THRU Beam support, which can achieve bone growth and expansion throughout the implantation process.  "We are pleased to announce the FLX platform, which represents the next development of STALIF technology," said John Viscogliosi, Chairman and CEO of Centinel Spine. 3D printing technology , We can offer the mature advantages of the STALIF design with truly novel all titanium lattice options. This allows our surgeons the flexibility to use a single instrument to use a variety of implant material options to solve each patient's unique pathological problems. The STALIF FLX integrated interbody fusion cage has advantages over other all titanium implants because they are specified for one or two consecutive levels of autograft or allograft bone grafts. Viscogliosi continues: 'This approval is a significant achievement in the development of 3D printed titanium alloy equipment because the 510(k) includes a series of intervertebral fusion devices representing thousands of potential Cervical and Lumbar fusion implants.  Prior to the establishment of Centinel Spine, Surgicraft introduced an innovative integrated combination device, which is a new type of implant for anterior spinal surgery. The device is implanted through a single incision, which is more than ever used More invasive technologies for these types of surgery. The FLX platform is the next step in the high-tech treatment of spinal disorders. The FDA-approved platform will bring Centinel closer to becoming the world leader in spinal therapy. Centinel Spine has 30 years of clinical experience. Experiences, including the work of Surgicraft and Raymedica, continue to use 3D printing and other advanced technologies to relieve pain and restore the patient's ability to move. Spinal conditions are some of the most painful and debilitating diseases that can affect the body, but due to technologies such as 3D printing and advanced materials, these diseases become easier to treat, and the pain and recovery time is the shortest. US Food and Drug Administration The approval of Centinel Spine's latest platform is another leap in the treatment of spinal diseases. |
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