The Johnson & Johnson Medical Devices Companies* today announced that DePuy Synthes has launched the CONDUIT Interbody Platform with EIT Cellular Titanium Technology, further expanding its comprehensive offering to treat degenerative spine disease.
| CHICAGO, Sept. 25, 2019 /PRNewswire/ -- The Johnson & Johnson Medical Devices Companies* today announced that DePuy Synthes has launched the CONDUIT Interbody Platform with EIT Cellular Titanium Technology, further expanding its comprehensive offering to treat degenerative spine disease. The innovative portfolio, which includes 3D printed titanium interbody implants for spinal fusion surgery is designed to mimic natural bone and help facilitate spinal fusion. The announcement was made at the 34th Annual North American Spine Society (NASS) meeting.
During spinal fusion, a degenerated, collapsed disc is removed and replaced with an interbody spacer along with bone graft with the goal of restoring natural height and alignment between two vertebrae. The concept is to replace the former mobile disc space between two vertebrae with an interbody spacer so that the segment fuses as a single, solid bone. Thanks to 3D printing, CONDUIT Implants are 80% porous—bringing a differentiated cellular structure designed to mimic the properties of bone1 and assist with intra and post-operative visualization2,3. The cellular structure has a modulus of elasticity, or change in stiffness, similar to bone4. All of these characteristics aim to help facilitate bone fusion. “My experience with CONDUIT has been in both the lumbar and cervical spine,” said Dr. Wilson Z. Ray, Neurological Surgeon, St. Louis, Missouri**. “The implant allows for superior visualization, virtually no scatter on CT scan and early fusion assessment as compared to other titanium interbody devices.” The launch of the CONDUIT Implants portfolio follows Johnson & Johnson Medical Devices Companies’ 2018 acquisition of Emerging Implant Technologies (EIT), a Germany-based developer of 3D printed technologies for spine procedures. The CONDUIT Implants join the recently launched ACIS ProTi 360° Anterior Cervical Interbody System Hyperlordotic Cages, which enhance the PROTI 360° Family of Implants. These platforms strengthen the company’s existing comprehensive portfolio of interbody cages, addressing a variety of surgical needs with a broad range of advanced materials. “Our goal as a spine business is to focus on the areas with the most potential to solve unmet clinical needs, and we are excited to add advanced materials to our interbody portfolio as another option for surgeons,” said Nadav Tomer, Worldwide President, Spine, DePuy Synthes****. “The launch of the CONDUIT portfolio, together with our comprehensive interbody implant offerings for degenerative disc disease, helps us deliver life-enhancing spine solutions that advance the standard of care for patients everywhere.” Several features of CONDUIT Implants include:
The CONDUIT Platform reinforces Johnson & Johnson’s commitment to 3D printing technology. In collaboration with our extensive network of partners, Johnson & Johnson is emerging as one of the leaders in 3D printing resulting in product design freedom, consumer and patient-specific product personalization, speed to market, global supply chain transformation and materials innovation. The CONDUIT Platform and PROTI 360° Family will be showcased at NASS as part of DePuy Synthes’ innovative solutions that address unmet needs for surgeons and patients in degenerative disc disease, deformity and complex cervical procedures. The company will also be showcasing enabling technologies, minimally invasive spine (MIS) solutions, and biomaterials to support these procedures, including SENTIO MMG for neuromonitoring, the VIPER PRIME System for MIS, and FIBERGRAFT Family of Products and ViviGen Cellular Bone Matrix biomaterials solutions. Through the company’s collaboration with Brainlab, DePuy Synthes also has the opportunity to feature Cirq Robotic Surgical Assistant, which is now FDA cleared as part of the Brainlab Spinal Navigation System including compatibility with EXPEDIUM and VIPER Systems for navigation in the U.S. About Johnson & Johnson Medical Devices Companies About DePuy Synthes Cautions Concerning Forward-Looking Statements This press release contains “forward-looking statements” as defined in the Private Securities Litigation Reform Act of 1995 regarding CONDUIT Interbody Platform with EIT Cellular Titanium Technology. The reader is cautioned not to rely on these forward-looking statements. These statements are based on current expectations of future events. If underlying assumptions prove inaccurate or known or unknown risks or uncertainties materialize, actual results could vary materially from the expectations and projections of DePuy Synthes, any of the other Johnson & Johnson Medical Devices Companies and/or Johnson & Johnson. Risks and uncertainties include, but are not limited to: uncertainty of commercial success; challenges to patents; competition, including technological advances, new products and patents attained by competitors; manufacturing difficulties and delays; product efficacy or safety concerns resulting in product recalls or regulatory action; changes to applicable laws and regulations, including global health care reforms; changes in behavior and spending patterns of purchasers of health care products and services; and trends toward health care cost containment. A further list and descriptions of these risks, uncertainties and other factors can be found in Johnson & Johnson’s Annual Report on Form 10-K for the fiscal year ended December 30, 2018, including in the sections captioned “Cautionary Note Regarding Forward-Looking Statements” and “Item 1A. Risk Factors,” and in the company’s most recently filed Quarterly Report on Form 10-Q, and the company’s subsequent filings with the Securities and Exchange Commission. Copies of these filings are available online at www.sec.gov, www.jnj.com or on request from Johnson & Johnson. Neither Johnson & Johnson Vision Care, Inc., the Johnson & Johnson Medical Devices Companies nor Johnson & Johnson undertakes to update any forward-looking statement as a result of new information or future events or developments. *Comprising the surgery, orthopedics, vision and interventional solutions businesses within Johnson & Johnson’s Medical Devices segment CIRQ is a registered trademark of Brainlab AG in Germany and/or the U.S. 1 VAL2016-043 Strut diameter summary rev 0 © DePuy Synthes 2019. All rights reserved.
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