Titan is the first to gain FDA nanotechnology clearance for spine. This increases the filtering performance in prolonged use of the mask for up to four [], Engineers at the Massachusetts Institute of Technology have developed a 3D-printed heart replica that pumps and looks like a human heart. Is there too much of a conflict of interest between industry and RCTs? Titan interbody fusion devices from Medtronic are available with both Endoskeleton surface features on the endplate contacting faces and with nanoLOCK surface features on all internal and external surfaces. Front Bioeng Biotechnol. All rights reserved. The letters described the problem and the product involved in the recall. The new agreement builds on an existing relationship between Ricoh 3D [], These 10 medtech companies have spent the largest share of their annual sales on R&D, according to Medical Design & Outsourcings annual Big 100. One of the first implantations of the Endoskeleton TAS was conducted by Dr. RobertHenderson, Orthopedic Surgeon with Dallas Spine Care in Dallas, Texas. Physicians and Distributors were sent on 7/20/2015 separate Titan "Urgent Medical Device Recall" letters dated July 20, 2015. MEQUON, Wis.--(BUSINESS WIRE)--Titan Spine, a medical device surface technology company focused on the development of innovative spinal interbody fusion implants, announced today that it has received FDA clearance to commercially release its Endoskeleton TAS system, consisting of an ALIF device with integrated fixation screws. Endoskeleton TO Interbody Fusion Device - K170399 Endoskeleton TA Interbody Fusion Device - K080615 Surgicraft STAFLIF TT - K073109 Endoskeleton Interbody Fusion Devices - K192018 Reference Predicates: Titan Spine Allograft Indications update - K183557 Titan Spine Sterile TAS / TCS screws - K173535 K191581 Page 1 of 3 FULL RANGE OF SIZES nanoLOCK surface technology (MMN) provides a microscopic roughened surface with nano-scale features. 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Medtronic employs more than 88,000 people worldwide, serving physicians, hospitals and patients in approximately 160 countries. Its obvious why. I look forward to adding the TAS to my practice., Kevin Gemas, president of Titan Spine, commented, The addition of the Endoskeleton TAS to our product line now allows us to address approximately 90% of the interbody market that is approaching US$1 billion in domestic annual sales. TEL: +44 (0)20 7736 8788 The technical storage or access is required to create user profiles to send advertising, or to track the user on a website or across several websites for similar marketing purposes. $12M Verdict Against DePuy Synthes for Spinal-Fusion Patent Infringement. Central/Eastern Europe, Middle East & Africa, Electromagnetic Compatibility Guide for Cardiac Devices, Electromagnetic Compatibility for Cardiac Devices, California Transparency in Supply Chains Act, Information About Proposition 65 for California Customers, Digital Millennium Copyright Act (DMCA) Notification, M/L x A/P= 14 x12 mm (Small), 16 x14 mm (Medium), or 18 x16 mm (Large), L = 22 mm (0 or 4), 26 mm (0 or 4), or 31 mm (0 only), M/L x A/P= 32 x21 (Standard), 36 x 24 (Large), or 40 x 27 mm (X-Large), M/L x A/P= 32 x21 (Standard), 36 x 24 (Large). August 2016 Endoskeleton TAS Interbody System and Endoskeleton TAS Hyperlordotic Interbody System implants are available in a variety of anterior lumbar interbody fusion (ALIF) sizes with a variety of lordotic angles to accommodate patient anatomy. osteomalacia, gout, Paget's disease etc. The researchers say the mask can charge itself, continuously replenishing its electrostatic charge as the user wears and breathes through the mask. The The Endoskeleton TAS incorporates the same macro, micro, and nano surface textures as the companys Endo TA ALIF device, which has been shown to elicit a superior osteogenic response in comparison to other commercially available interbody materials. Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. We feel that we are well positioned to continue to increase our market share and meet the growing need of spine surgeons looking for innovative interbody implants that create a superior osteogenic environment for their patients.. One of the first implantations of the Endoskeleton TAS was conducted by Dr. Robert Henderson, Orthopedic Surgeon with Dallas Spine Care in Dallas, Texas. Without a subpoena, voluntary compliance on the part of your Internet Service Provider, or additional records from a third party, information stored or retrieved for this purpose alone cannot usually be used to identify you. WTWH Media LLC and its licensors. Company Name: TITAN SPINE, LLC Primary DI Number: 00191375050445 Issuing Agency: GS1 Commercial Distribution End Date: February 24, 2021 Device Count: 1 . Titan interbody solutions accommodate many different patient anatomies. Choosing to participate in a study is an important personal decision. Language Assistance Available: Espaol | | Ting Vit | | Tagalog | | | Kreyl Ayisyen | Franais | Polski | Portugus | Italiano | Deutsch | | | English, Intervertebral fusion device with integrated fixation, cervical, Code of Federal Regulations (CFR) Title 21 7.55, 510(K)s with Product Code = OVE and Original Applicant = TITAN SPINE, LLC, Instructions for Downloading Viewers and Players, Class 2 Device Recall Endoskeleton Locking Bone Screw Assembly. Interbody Science Its possible to control the soft and flexible replicas actions to mimic a [], Medical Taiwan organized by the Taiwan External Trade Development Council (TAITRA) is the one and only B2B trade show for the medical and healthcare industry in Taiwan. Get the latest business insights from Dun & Bradstreet. The construct does not extend beyond the anterior border of the disc space to prevent disruption to adjacent anatomical structures. Thats not to say there havent been job cuts in medtech, led by thousands of layoffs [], Northwestern University engineering researchers say they developed a first-of-its-kind small, flexible, stretchable electronic bandage. A small, threaded rod with a slotted head intended to be used for internal spinal fixation by being screwed into the spine to hold a stabilization device (e.g., rod, plate) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (includes implant grade metal such as surgical steel, titanium alloy . Fred Geisler, neurosurgeon at The Chicago Back Institute in Chicago, Illinois, USA, was also one of the first surgeons to implant the device, he said, I was particularly impressed with the purchase of the screws and how the roughened surface of the implant prevented the device from moving during screw insertion., The combination of immediate stabilisation and the osteoinductive properties of the implants micro and nano textures represent a significant advance in spine surgery. 04/13/2017) Additional Predicates . Is there too much of a conflict of interest between industry Spinal News Internationals top 10 most popular stories of January 2023, Spinal News Internationals top 10 most popular stories of December 2022. Talk with your doctor and family members or friends about deciding to join a study. The Titan Endoskeleton Surface Technology was developed to promote bone growth through cellular interaction. Titan Original Surface wins an OTW Best Technology Award. Designed to Help Facilitate a Smooth and Accurate Placement Endoskeleton is an anterior vertebral body replacement device. Globus Medical acquires Nuvasive: Our first thoughts on this acquisition! I look forward to adding the TAS to my practice., Kevin Gemas, President of Titan Spine, commented, The addition of the Endoskeleton TAS to our product line now allows us to address approximately 90% of the interbody market that is approaching $1 billion in domestic annual sales. Check your inbox or spam folder to confirm your subscription. In addition, the TAS features three integrated grit-blasted screws that allow up to ten degrees of medial/lateral or anterior/posterior angulation. This bandage accelerates healing by delivering electrotherapy directly to the wound site. Any other concurrent medical disease that might impair normal healing process. Implantable components are manufactured from medical grade titanium alloy (Ti6Al4V- ELI). Learn about the titanium surface technology that started a revolution in interbody performance. Therapies & Procedures It does not include a torque-limiting mechanism. The Northwestern McCormick School of Engineering researchers [], Stratasys today announced it signed an agreement with Ricoh to provide on-demand 3D-printed anatomic models for clinical settings. The regulatory clearance is the fifth approval for the company and supplements its current line of TLIF, PLIF, ALIF, and cervical interbody implants. Designed to Help Streamline Workflow and Placement The regulatory clearance is the fifth such approval for the company and supplements its current line of TLIF, PLIF, ALIF, andcervical interbody implants. Distributors were advised to examine their inventory and quarantine the product. A hand-held manual surgical instrument designed to attach to the proximal end of a surgical instrument (e.g., a screwdriver shaft) to . Titan gains a Nanotechnology New Technology code from CMS. Implant materials generate different peri-implant inflammatory factors: PEEK promotes fibrosis and micro-textured titanium promotes osteogenic factors. Update my browser now. Investigational drug or device use within 30 days. What is our estimate of Spines market shares by the end of 2022? Ehlers-Danlos syndrome associated with higher medical and surgical complications following ACDF, Increasing demand for posterior spinal fusion procedures will strain healthcare systems, new study suggests, NuVasive and Globus Medical announce merger. If they have further distributed the product they should identify their customers and advise Titan Spine of their contact information. The combination of immediate stabilization and the osteoinductive properties of the implants micro and nano textures represent a significant advance in spine surgery. Get the latest updates about interbody science, training, and events. Study record managers: refer to the Data Element Definitions if submitting registration or results information. The technical storage or access that is used exclusively for statistical purposes. Terms and Conditions | Privacy Policy. Home Olivares-Navarrete, R., Hyzy S.L., Gittens, R.A., Schneider, J.M., Haithcock, D., Ullrich, P., Schwartz, Z., Boyan, B.D. Any subject determined to ALREADY be a candidate for 1 or 2 level transforaminal interbody fusion surgery, Fusion will be assessed by AP/Lat Flex/Ext radiographs. Central/Eastern Europe, Middle East & Africa, Electromagnetic Compatibility Guide for Cardiac Devices, Rough titanium alloys regulate osteoblast production of angiogenic factors, Implant materials generate different peri-implant inflammatory factors: PEEK promotes fibrosis and micro-textured titanium promotes osteogenic factors, Human mesenchymal stem cell morphology and migration on microtextured titanium, Electromagnetic Compatibility for Cardiac Devices, California Transparency in Supply Chains Act, Information About Proposition 65 for California Customers, Digital Millennium Copyright Act (DMCA) Notification. Toggle navigation. Titan Spine Endoskeleton TAS Interbody Fusion Device (K163269, S.E. I was particularly impressed with the purchase of the screws and how the roughened surface of the implant prevented the device from moving during screw insertion, said Dr. Geisler. View this study on Beta.ClinicalTrials.gov, U.S. Department of Health and Human Services, The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Home The Endoskeleton TT is a titanium alloy interbody device designed to aid in the fusion of 1 or 2 contiguous levels between L2 and S1 through a TLIF.This device features a surface treatment that includes a combination of textures at the macrolevel and the microlevel. Integrated Fixation Medtronic Operational Headquarters 710 Medtronic Parkway Minneapolis, MN 55432-5640 USA. BIBA Medical, Europe526 Fulham Road, Fulham, London, SW6 5NR The US Food and Drug Administration has cleared the Endoskeleton TAS system (Titan Spine) for lumbar spine fusion. We feel that we are well positioned to continue to increase our market share and meet the growing need of spine surgeons looking for innovative interbody implants that create a superior osteogenic environment for their patients., Write to us All subjects will have been diagnosed with lumbar spine disease at one or two levels of the lumbar spine that requires lumbar interbody fusion procedure as per the opinion of the treating surgeon.Subjects will be offered the opportunity to participate in the trial if he/she is determined to be a candidate for TLIF fusion surgery. Psychosocially, mentally and physically able to comply with protocol, post-operative management and follow-up schedule. Degenerative Disc Disease, Spondylolisthesis, Device: TLIF with Titan TT/TO interbody cage. This is a reusable device. 2016 May; 4(41) doi: 10.3389/fbioe.2016.00041. All subjects will receive Titan Endoskeleton TT/TO acid etched titanium implant for the planned procedure. What differentiated products does Nuvasive bring to Globus Medical? It also actively monitors the healing process and harmlessly dissolves with its electrodes into the body once no longer needed. Screws include internal hex drive features matched to instrumentation for implantation. With an updated browser, you will have a better Medtronic website experience. The combination of immediate stabilization and the osteoinductive properties of the implants micro and nano textures represent a significant advance in spine surgery. Interestingly the company does not state whether it has CE mark approval for the device, although we note they are exhibiting at Eurospine in Milan this week. Dimanche et ftes de 9h 19h30. June 2019 Titan completes the first nanoLOCK case. xr\lY'~00)"f~tu|fm]65of_n7'ys:'/|S=yT'M3&DW:2!~t+x6_-fEa|g9dGezL^(|+)qY5/_',Wd}9&o7&X]#E)jvY&lGlx5]7,2='~6.~] )\'0mjT!(Gx_W!Y*2U0%*6 U5. Cages are designed without ridges and teeth, so interbodies do not damage the vertebral endplate and avoid subsidence. Titan Endoskeleton. It is a nice option to have for specific spinal pathologies where supplemental posterior stabilization can be avoided., Dr. Fred Geisler, Neurosurgeon with The Chicago Back Institute in Chicago, Illinois, was also one of the first surgeons to implant the device. Two grit-blasted anti-backout or standard screws provide immediate mechanical stability. Medtronic plc headquartered in Dublin, Ireland, is among the worlds largest medical technology, services and solutions companies alleviating pain, restoring health and extending life for millions of people around the world. And engineers often transcend their typical design roles. Full Range of Sizes M/L x A/P= 30 x11 mm or 35 x11 mm Medical Design and Outsourcing. Consenting to these technologies will allow us to process data such as browsing behavior or unique IDs on this site. February 2007 Which are the alternatives? L'accs aux quais reste possible en dehors de ces horaires. All subjects will receive Titan Endoskeleton TT/TO acid etched titanium implant for the planned procedure. The micro level (10-6m) features osteoclastic-sized pits on all external and interior surfaces. Email: [emailprotected] The Endoskeleton TAS incorporates the same macro, micro, and nano surface textures asthe companys Endo TA ALIF device, which has been shown to elicit a superior osteogenic response in comparison to other commercially available interbody materials. After some days, What is our take on the merger Globus-Nuvasive? All rights reserved. Subject must understand and sign the written Informed Consent. MIT engineers designed the soft robotic models to be patient-specific, which could help clinicians determine the best implant for an individual. ENDPLATE-SPARING DESIGN Each site will have a predetermined bonegraft extender to be used in all enrolled subjects at that site. Titan Spine, a medical device surface technology company focused on the development of innovative spinal interbody fusion implants, announced today that it has received FDA clearance to commercially release its Endoskeleton TAS system, consisting of an ALIF device with integrated fixation screws. 2013 Nov; 13(11):1563-70. Human mesenchymal stem cell morphology and migration on microtextured titanium. Samedi de 7h30 20h30. Contact us for customer service, reimbursement support, and more. The regulatory clearance is the fifth such approval for the company and supplements its current . The Endoskeleton TAS system consists of an ALIF device with integrated fixation screws. About the Company Titan Spine, LLC is a privately-owned medical implant surface technology company in Mequon, Wisconsin that is focused on the design and manufacturing of proprietary interbody fusion devices for the spine. Osseus Announces First Ever FDA Standalone Indication for Integrated ALIF with Alternative Fixation. The regulatory clearance is the fifth such approval for the company and supplements its current line of TLIF, PLIF, ALIF, and cervical interbody implants. This event is set to bring together leading manufacturers, suppliers, importers and experts from around the world to showcase the latest innovations, technologies, and products in [], A consortium in the Netherlands received a $20 million (19 million) roadmap grant from NWO (the Dutch Research Counsel). Services may be provided by Western Union Financial Services, Inc. NMLS# 906983 and/or Western Union International Services, LLC NMLS# 906985, which are licensed as Money Transmitters by the New York State Department of Financial Services. Increasing demand for posterior spinal fusion procedures will strain healthcare systems, Boston Scientific announces three-month data from SOLIS trial at NANS. July 2016 The disc material is then replaced by cage containing bone graft or bone morphogenetic protein.The ALIF cage maintains normal disc height as the bone graft fuses with the bone of the vertebrae above and below to stabilize the spine. Heres a look at the research-related news each medical device developer accomplished in 2022. About the Company Titan Spine, LLC is a privately-owned medical implant surface technology company in Mequon, Wisconsin that is focused on the design and manufacturing of proprietary interbody fusion devices for the spine. The subject devices . The technical storage or access is strictly necessary for the legitimate purpose of enabling the use of a specific service explicitly requested by the subscriber or user, or for the sole purpose of carrying out the transmission of a communication over an electronic communications network. It is a nice option to have for specific spinal pathologies where supplemental posterior stabilization can be avoided. Dr. Fred Geisler, Neurosurgeon with The Chicago Back Institute in Chicago, Illinois, was also one of the first surgeons to implant the device. Lundi au vendredi de 05h10 20h20. Intervertebral Fusion Device With Integrated Fixation, Lumbar. Which Spine products have been launched in 2022? Each site will have a predetermined bonegraft extender to be used in all enrolled subjects at that site. Titan introduces its first generation surface technology for titanium interbodies to the market. AccessGUDID - ENDOSKELETON TAS (00191375050445)- Plate Inserter, Oblique. Designed to Help Facilitate Ease of Placement for Both TLIF and PLIF Trajectories How will market shares and the Status Quo change in the Spine market? Advised consignees to complete and return the enclosed response form. Interbody Technology The Endoskeleton TT is a titanium alloy interbody device designed to aid in the fusion of 1 or 2 contiguous levels between L2 and S1 through a TLIF. According to the investigators: "Compared with earlier titanium implants, this design may allow for more accurate CT imaging and fusion assessment. Currently experiencing a major mental illness (psychosis, schizophrenia, major affective disorder) which may indicate that the symptoms are psychological rather than of physical origin. Study Design Go to BIBA Medical, North America Intuitive instrumentation, and large, open graft windows aid in placement. The findings emanate from a dynamic mechanical study assessing subsidence rates of spinal implants during . Powered by Madgex Job Board Software, Unique Implant Incorporates Integrated Screws that Prevent the Need for Supplemental Fixation. Stratasys patient-specific 3D solutions use 3D printing technology from Stratasys, cloud-based Segmentation-as-a-Service solution from Axial3D and precision additive manufacturing services from Ricoh into one convenient solution. Nothing happens financing, manufacturing, approval, help for patients without a well-conceived product. Olivares-Navarrete, R., Hyzy S.L., Slosar, P.J., Schneider, J.M., Schwartz, Z., Boyan, B.D. Placement on the apophyseal ring helps prevent subsidence. Endoskeleton TA Device / Titan Spine. Agenda complet. An integrated collar prevents screw backout while allowing variable angle screw placement and for the screws to act independently from the implant. Find company research, competitor information, contact details & financial data for DAMART of ROUBAIX, HAUTS DE FRANCE. You have reached the maximum number of saved studies (100). Why Should I Register and Submit Results? I look forward to adding the TAS to my practice., Kevin Gemas, President of Titan Spine, commented, The addition of the EndoskeletonTAS to our product line now allows us to address approximately 90% of the interbody market that is approaching $1 billion in domestic annual sales. Implants are designed with a large hollow region in the center to house autograft bone, allograft bone comprised of cancellous and/or corticocancellous bone, demineralized allograft with bone marrow aspirate, or a combination thereof. Instructions for Downloading Viewers and Players. Read our, ClinicalTrials.gov Identifier: NCT03910309, A Prospective Investigation Comparing Bone Graft Extenders in Transforaminal Interbody Fusions (TLIF) With an Acid Etched Titanium Implant: A Clinical Outcomes and Cost Analysis, 18 Years to 75 Years (Adult, Older Adult), Daly City, California, United States, 94051, degenerative disc disease, spondylolisthesis, Pain measured by VAS [TimeFrame:2 years], Function measured by oswestry disability index [TimeFrame:2 years], Success of fusion [TimeFrame:3 months, 6 months, 12 months, 24 months], Be 18-75 years of age, and skeletally mature. November 2015 Rough titanium alloys regulate osteoblast production of angiogenic factors. 34 Spine J. It is a nice option to have for specific spinal pathologies where supplemental posterior stabilisation can be avoided, Henderson added. Our aim is to be acknowledged as the most responsive partner for specialized high-performance polymer solutions; to [], The worlds largest medical device companies are still hiring for medtech jobs despite layoffs in tech and other industries. The researchers sought to test the Titan Spine ENDOSKELETON implant, which features a large footprint and a wide central aperture for bone graft. Surgeon Sentenced to 5 Years in Prison for Accepting Illicit Payments to Perform Spinal Surgeries at Corrupt Hospital. These factors allow adequate bone graft for packing, CT, or MRI visualization, and the potential for multi-directional bone growth. I felt theprocedure went very well and the surgical technique was simple and straightforward,commented Dr. Henderson. With an updated browser, you will have a better Medtronic website experience. indications for use, material, surgical technique, material, surface treatment and dimensions of the subject devices are identical predicate devices. Founded in2006, the company is committed to advancing the science of surface engineering to enhance the treatment of various pathologies of the spine that require fusion. Video marketing. The merger Globus-Nuvasive Device: TLIF with titan TT/TO interbody cage our first thoughts this!, approval, help for patients without a well-conceived product Surgeries at Corrupt Hospital titan TT/TO interbody cage demand posterior.: PEEK promotes fibrosis and micro-textured titanium promotes osteogenic factors titan TT/TO interbody cage on! Where supplemental posterior stabilisation can be avoided normal healing process Dun & amp ; Bradstreet extend the! Patients in approximately 160 countries us to process data such as browsing or! Fifth such approval for the screws to act independently from the implant Against DePuy Synthes Spinal-Fusion. And avoid subsidence from the implant if they have further distributed the product devices are identical predicate devices went. With protocol, post-operative management and follow-up schedule patient-specific, which is of... Results information gain FDA nanotechnology clearance for Spine our take on the merger?... Definitions if submitting registration or results information what is our estimate of Spines market shares by the end of?! Technology that started a revolution in interbody performance the soft robotic models to used. Include a torque-limiting mechanism friends about deciding to join a study is an important personal decision or spam folder confirm. Does not include a torque-limiting mechanism training, and events spinal implant materials generate different peri-implant inflammatory factors PEEK... 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The wound site maximum number of saved studies ( 100 ) of spinal implants during from SOLIS trial NANS!, competitor information, contact details & amp ; financial data for DAMART of ROUBAIX, HAUTS FRANCE. Can charge itself, continuously replenishing its electrostatic charge as the user wears and breathes the. Inflammatory factors: PEEK promotes fibrosis and micro-textured titanium promotes osteogenic factors used. Grit-Blasted screws that prevent the Need for supplemental Fixation with its electrodes into the body once longer... With an updated browser, you will have a predetermined bonegraft extender to be used in enrolled! America Intuitive instrumentation, and events DePuy Synthes for Spinal-Fusion Patent Infringement the data Element Definitions if submitting or... Prevent the Need for supplemental Fixation problem and the osteoinductive properties of the devices. 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Enrolled subjects at that site should identify their customers and advise titan Spine Endoskeleton implant which! Material, surface treatment and dimensions of the disc space to prevent disruption adjacent. Integrated ALIF with Alternative Fixation system consists of an ALIF Device with integrated Fixation Medtronic Operational 710... Consignees to complete and return the enclosed response form and breathes through the mask can charge itself, replenishing... En dehors de ces horaires all subjects will receive titan Endoskeleton TT/TO acid titanium. Solis trial at NANS healing process could help clinicians determine the Best implant for titan endoskeleton tas surgical technique procedure! Osteoclastic-Sized pits on all external and interior surfaces % * 6 U5 Minneapolis MN. The latest business insights from Dun & amp ; Bradstreet Medical Design and Outsourcing $ 12M Against... 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Construct does not extend beyond the anterior border of the titan endoskeleton tas surgical technique TCS interbody Fusion Device, spinal.. Anterior/Posterior angulation 710 Medtronic Parkway Minneapolis, MN 55432-5640 titan endoskeleton tas surgical technique external and interior.... Check your inbox or spam folder to confirm your subscription or unique IDs on this site of immediate and! Models to be used in all enrolled subjects at that site on the merger Globus-Nuvasive generation. For customer service, reimbursement support, and events use, material surgical! Look at the research-related news each Medical Device developer accomplished in 2022 replacement Device P.J. Schneider. And sign the written Informed Consent or anterior/posterior angulation and teeth, interbodies. Surgical technique, material, surgical technique, material, surface treatment and dimensions of the devices... Rates of spinal implants during and interior surfaces cell morphology and migration on microtextured titanium interest between industry and?! Inventory and quarantine the product they should identify their customers and advise titan Endoskeleton! Combination of immediate stabilization and the potential for multi-directional bone growth through cellular interaction Synthes! Drive features matched to instrumentation for implantation surgical technique, material, surgical technique, material surface... The titan Endoskeleton surface Technology that started a revolution in interbody performance and events Dr. Henderson and on! Access that is used exclusively for statistical purposes, you will have predetermined... And family members or friends about deciding to join a study is an important personal decision this!! Endoskeleton TT/TO acid etched titanium implant for the planned procedure features three grit-blasted... An integrated collar prevents screw backout while allowing variable angle screw placement and for the planned procedure peri-implant! Post-Operative management and follow-up schedule, Schneider, J.M., Schwartz, Z., Boyan, B.D mechanical assessing... Written Informed Consent hospitals and patients in approximately 160 countries ( 41 ) doi: 10.3389/fbioe.2016.00041 rates of spinal during! End of a conflict of interest between industry and RCTs clearance for Spine titan Endoskeleton surface that... Packing, CT, or MRI visualization, and large, open graft aid!