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. Designed to Help Facilitate Ease of Placement for Both TLIF and PLIF Trajectories This is a prospective, multi-center controlled observational clinical study. 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. A hand-held manual surgical instrument designed to attach to the proximal end of a surgical instrument (e.g., a screwdriver shaft) to allow the surgeon to perform manipulations with the instrument, typically manual rotation of a bone screw or tensioning of a nut during a surgical procedure. Titan Endoskeleton TT and OsteoSponge/BMA. The design incorporates windows through the implant to permit visualization of the graft material, and over time, formation of new bone. L'accs aux quais reste possible en dehors de ces horaires. July 2016 BIBA Medical, Europe526 Fulham Road, Fulham, London, SW6 5NR The most comprehensive information guide on ENDOSKELETON TAS - TITAN SPINE LLC including impacted physicians & ROI, Business Case, HEOR & VAC Business & Quality Metrics. Email: [emailprotected] Find company research, competitor information, contact details & financial data for DAMART of ROUBAIX, HAUTS DE FRANCE. spinemarketgroup@gmail.com info@thespinemarketgroup.com. Aimed initially at the purification of viral vectors used for cell and gene [], Hear from Medtech Colors 10 Pitch Competition finalists; Kwame Ulmer joins us for the Newsmakers. Medical Devices companies use Gridlex Zip Help Desk, Customer Services, Shared Mailbox and Ticketing system to manage Medical Device customer support, quality, safety, complaints and ordering, and other operations, Hospital Reimbursement & Quality Outcomes, TITAN SPINE LLC - ENDOSKELETON TAS : Product Information, TITAN SPINE LLC - ENDOSKELETON TAS : Product Code Information, Labeling does not contain MRI Safety Information. Choosing to participate in a study is an important personal decision. Titan gains a Nanotechnology New Technology code from CMS. One hundred and fifty (150) subjects will participate in the study at a max of 15 clinical sites. Titan completes the first nanoLOCK case. Heres a look at the research-related news each medical device developer accomplished in 2022. Lundi au vendredi de 05h10 20h20. 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. Three integrated, grit-blasted screws provide immediate mechanical stability. 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. The regulatory clearance is the fifth approval for the company and supplements its current line of TLIF, PLIF, ALIF, and cervical interbody implants. Osseus Announces First Ever FDA Standalone Indication for Integrated ALIF with Alternative Fixation. 203 0 obj <>stream Designed to Help Facilitate a Smooth and Accurate Placement According to the investigators: "Compared with earlier titanium implants, this design may allow for more accurate CT imaging and fusion assessment. Screws include internal hex drive features matched to instrumentation for implantation. 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. 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. The device is typically made of metal and/or synthetic material (e.g., polysulphone) and may have a straight or T-shaped handle grip which may include additional features such as a ratchet mechanism to allow the surgeon to maintain a constant hold on the handle when providing rotation in one direction. Therapies & Procedures 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.. 2015 Mar; 40(6): 399-404. Study Design Go to Implantable components are manufactured from medical grade titanium alloy (Ti6Al4V- ELI). Designed to Accommodate Optimal TLIF Placement An integrated collar prevents screw backout while allowing variable angle screw placement and for the screws to act independently from the implant. %PDF-1.7 % Anterior lumbar interbody fusion (ALIF) is a spine surgery that involves approaching the spine from the front of the body to remove disc or bone material from in between two adjacent lumbar vertebrae. How are the Top Spine Companies performing in 2022 so far? The regulatory clearance is the fifth such approval for the company and supplements its current . The regulatory clearance is the fifth such approval for the company and supplements its current line of TLIF, PLIF, ALIF, andcervical interbody implants. Intuitive instrumentation, and large, open graft windows aid in placement. Devices incorporate Titan Surface Technologies, where superior and inferior surfaces include either Chemtex or nanoLOCK surface treatments (MMN) designed to improve fixation to the adjacent bone. Medtronic Operational Headquarters 710 Medtronic Parkway Minneapolis, MN 55432-5640 USA. Dimanche et ftes de 9h 19h30. 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. Titan becomes the first to offer surface technology on a lateral interbody device. TEL: +1 949 723 9309 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.. All subjects will receive Titan Endoskeleton TT/TO acid etched titanium implant for the planned procedure. 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. Spinal & Orthopaedic 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. Cages are designed without ridges and teeth, so interbodies do not damage the vertebral endplate and avoid subsidence. Talk with your doctor and family members or friends about deciding to join a study. Olivares-Navarrete, R., Hyzy S.L., Slosar, P.J., Schneider, J.M., Schwartz, Z., Boyan, B.D. The radiopaque nature of titanium assists in device placement. Two inserter designs that accommodate straight and curved attachment, final positioning instrumentation, and a smooth leading implant edge allow for ease of insertion for the TLIF approach. I am pleased Titan has added the supplemental fixation feature to its ALIF device that I have been using with great success to date. Medical Design and Outsourcing. 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). Ghost Productions provided Titan Spine with an technique animation of its Endoskeleton device. Spine. Endoskeleton TAS ALIF VIDEO ANIMATION (Old version of Titan Spine) These designs support anterior cervical and anterior, posterior, oblique, and lateral approaches to the lumbar spine. Instructions for Downloading Viewers and Players. Medtech developers and medtech jobs are resilient, with the industrys COVID-19 pandemic performance only bolstering its recession-proof reputation. Designed to Simplify Anterior Workflow & Placement Titan Spine is touting the results of a new study demonstrating a reduced subsidence rate and overall subsidence amount of its Endoskeleton TA device compared to a commercially available PEEK device. 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 Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant. ), Osteoporosis defined as a DEXA bone density measurement T score 2.5 (Necessity for DEXA scan will be determined by investigator's standard of care). The Titan Endoskeleton surface uses subtractive manufacturing to create unique textures at the macro and micro levels. The combination of immediate stabilization and the osteoinductive properties of the implants micro and nano textures represent a significant advance in spine surgery. LARGE WINDOWS AND INTERNAL VOLUMES Titan Endoskeleton. Designed to Help Streamline Workflow and Placement Titan Spine If they have further distributed the product they should identify their customers and advise Titan Spine of their contact information. November 2015 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. Interbody Technology The US Food and Drug Administration has cleared the Endoskeleton TAS system (Titan Spine) for lumbar spine fusion. indications for use, material, surgical technique, material, surface treatment and dimensions of the subject devices are identical predicate devices. Degenerative Disc Disease, Spondylolisthesis, Device: TLIF with Titan TT/TO interbody cage. Not consenting or withdrawing consent, may adversely affect certain features and functions. Titan introduces its first generation surface technology for titanium interbodies to the market. Study record managers: refer to the Data Element Definitions if submitting registration or results information. Note: If you need help accessing information in different file formats, see Create and promote branded videos, host live events and webinars, and more. Agenda complet. Distributed in the states of CA, TX, OK, MA, NY, IN, OR, and GA. 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. Founded in 2006, the company is committed to advancing the science of surface engineering to enhance the treatment of various pathologies of the spine that require fusion. Titan Original Surface wins an OTW Best Technology Award. Advertising: Michael Broughton [emailprotected], United Kingdom: Spine J. May also have spondylosis, spinal stenosis, or spondylolisthesis at these levels. 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.~] Home These factors allow adequate bone graft for packing, CT, or MRI visualization, and the potential for multi-directional bone growth. A hand-held manual surgical instrument designed to attach to the proximal end of a surgical instrument (e.g., a screwdriver shaft) to . After some days, What is our take on the merger Globus-Nuvasive? In vitro studies indicate that this surface may upregulate significantly critical bone growth factors necessary for fusion. I am pleased Titan has added the supplemental fixation feature to its ALIF device that I have been using with great success to date. Currently experiencing a major mental illness (psychosis, schizophrenia, major affective disorder) which may indicate that the symptoms are psychological rather than of physical origin. Get the latest updates about interbody science, training, and events. Efficient surgical workflow, intuitive instrumentation, and a smooth leading implant edge allow for easy insertion for the TLIF and PLIF trajectories. With an updated browser, you will have a better Medtronic website experience. Home Update my browser now. "I am pleased to initiate use of Titan Spine's Endoskeleton TAS interbody device and its specialised surface treatment," comments Sutcliffe. Skip to Main Content; National Library of Medicine NLM Tools and Resources FDA UDI Home FDA Medical Devices Home . Therapies & Procedures Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03910309. Have clinical and radiological evidence of degenerative disc disease at one or two levels of the lumbar spine between L2-S1. FULL RANGE OF SIZES To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. 2013 Nov; 13(11):1563-70. Banik, B., Riley, T., Platt, C., Brown, J. Unique Implant Incorporates Integrated Screws that Prevent the Need for Supplemental Fixation 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 . Please remove one or more studies before adding more. The construct does not extend beyond the anterior border of the disc space to prevent disruption to adjacent anatomical structures. The Endoskeleton TAS system consists of an ALIF device with integrated fixation screws. 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. Information provided by (Responsible Party): This is a prospective, multi-center controlled observational clinical study. New bone formation through the implant is intended to provide long-term structural support and fusion at the implanted disc space. The population will be drawn from an existing patient population per participating site. I felt theprocedure went very well and the surgical technique was simple and straightforward,commented Dr. Henderson. Was the Globus Medical merge with Nuvasive an expensive deal? MIT engineers designed the soft robotic models to be patient-specific, which could help clinicians determine the best implant for an individual. Rough titanium alloys regulate osteoblast production of angiogenic factors. 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. 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. Update my browser now. February 2007 (G]6/o7Y|>y*\tMJ}f+)W. Powered by Madgex Job Board Software, Unique Implant Incorporates Integrated Screws that Prevent the Need for Supplemental Fixation. The material on this site may not be reproduced, distributed, transmitted, cached or otherwise used, except with the prior written permission of WTWH Media. Solutions . RADIOPACITY Listing a study does not mean it has been evaluated by the U.S. Federal Government. BIBA Medical, North America 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. Implant designs for a variety of approaches. Healthcare Professionals 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. 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. The Endoskeleton lumbosacral interbody fusion devices are indicated for use in skeletally mature patients with Degenerative Disc Disease (DDD) at one or two contiguous levels from L2-S1; Endoskeleton cervical interbody fusion devices are indicated for use for anterior cervical interbody fusion in skeletally mature patients with degenerative disc All rights reserved. nanoLOCK surface technology (MMN) provides a microscopic roughened surface with nano-scale features. 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. Is there too much of a conflict of interest between industry and RCTs? November 2014 Titan is the first to gain FDA nanotechnology clearance for spine. It is a nice option to have for specific spinal pathologies where supplemental posterior stabilisation can be avoided, Henderson added. CorMatrix ECM gains FDA approval for Carotid Repair, Successful US implants of ValveXchange two-part heart valve system: Eu trials planned. "It is my belief that surface technology is the next significant innovation for spinal fusions due to the ability to affect a cellular response that promotes a more favourable osteogenic . Endoskeleton TA Device / Titan Spine. Each site will have a predetermined bonegraft extender to be used in all enrolled subjects at that site. hZko+1Aor'^#m`Mx Kl~F@3>.s$TJHCE+gR*Z>Xo"*:K*uU2sh*X9_ ?. Surgeon Sentenced to 5 Years in Prison for Accepting Illicit Payments to Perform Spinal Surgeries at Corrupt Hospital. 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. Implant materials generate different peri-implant inflammatory factors: PEEK promotes fibrosis and micro-textured titanium promotes osteogenic factors. Led by the Donders Institute for Brain, Cognition and Behaviour (Radboud University), the consortium aims to build a high-level MRI scanner. Endoskeleton is an anterior vertebral body replacement device. Get more details on current Medtronic interbodies. Hyperlordotic implants are those defined by a lordotic angle 16. 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). Advised consignees to complete and return the enclosed response form. 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. 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. The micro level (10-6m) features osteoclastic-sized pits on all external and interior surfaces. Which are the alternatives? 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. Increasing demand for posterior spinal fusion procedures will strain healthcare systems, Boston Scientific announces three-month data from SOLIS trial at NANS. 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 . With an updated browser, you will have a better Medtronic website experience. Get the latest business insights from Dun & Bradstreet. 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. Healthcare Professionals Front Bioeng Biotechnol. The combination of immediate stabilization and the osteoinductive properties of the implants micro and nano textures represent a significant advance in spine surgery. $12M Verdict Against DePuy Synthes for Spinal-Fusion Patent Infringement. Get the latest updates about interbody science, training, and events. 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. The findings emanate from a dynamic mechanical study assessing subsidence rates of spinal implants during . The regulatory clearance is the fifth approval for the company and supplements its current line of TLIF, PLIF, ALIF, and cervical interbody implants. Gare. 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. Human mesenchymal stem cell morphology and migration on microtextured titanium. Titan interbody solutions accommodate many different patient anatomies. Psychosocially, mentally and physically able to comply with protocol, post-operative management and follow-up schedule. I am pleased Titan has added the supplemental fixation feature to its ALIF device that I have been using with great success to date. K173535 Page 2 of 3. differ from the predicate devices in the . The technical storage or access that is used exclusively for anonymous statistical purposes. J&J subsidiary DePuy Synthes to pay $9.75M to resolve kickback allegations. Insert pedicle screws more precisely and safely without a robot or navigation system? One of the first implantations of the Endoskeleton TAS was conducted by Dr. RobertHenderson, Orthopedic Surgeon with Dallas Spine Care in Dallas, Texas. Samedi de 7h30 20h30. The technical storage or access is necessary for the legitimate purpose of storing preferences that are not requested by the subscriber or user. June 2019 Steve Cichy, 866-822-7800 Each year, Medical Design & Outsourcingranks the worlds largest 100 medical device companies based on annual revenue. [], A research team at City University of Hong Kong (CityU) says it engineered a breath-to-charge electrostatic face mask. United States: 34 This breakthrough inspired a revolution in surface technology, leading directly to a proprietary combination of textures that altered the interbody fusion market. Part Numbers / Product Description: 5302-3514 / 03.5 x 14mm Locking Screws; Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'. Dr Kingsley R Chin Warns Against Expert Surgeon Witnesses Supporting Copycat Pedicle Screw Lawsuits. 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. Its obvious why. TITAN ENDOSKELETON TT Approach: TLIF Designed to Accommodate Optimal TLIF Placement Two inserter designs that accommodate straight and curved attachment, final positioning instrumentation, and a smooth leading implant edge allow for ease of insertion for the TLIF approach. www.titanspine.com, 1985 - 2023 BioSpace.com. Any other concurrent medical disease that might impair normal healing process. 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. Robert Henderson, orthopaedic surgeon at Dallas Spine Care in Dallas, Texas, USA, performed one of the first implantations of the Endoskeleton TAS, he commented, I felt the procedure went very well and the surgical technique was simple and straightforward.. Company Name: TITAN SPINE, LLC Primary DI Number: 00191375050445 Issuing Agency: GS1 Commercial Distribution End Date: February 24, 2021 Device Count: 1 . The letters described the problem and the product involved in the recall. Physicians and Distributors were sent on 7/20/2015 separate Titan "Urgent Medical Device Recall" letters dated July 20, 2015. Le Gymnase CDCN uvre depuis quarante ans au soutien et au maillage du secteur chorgraphique sur la mtropole lilloise, ainsi que sur le territoire rgional et national. Investigational drug or device use within 30 days. 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. Physicians and Distributors were sent on 7/20/2015 separate Titan "Urgent Medical Device Recall" letters dated July 20, 2015. The regulatory clearance is the fifth such approval for the company and supplements its current line of TLIF, PLIF, ALIF, and cervical interbody implants. Medtronic employs more than 88,000 people worldwide, serving physicians, hospitals and patients in approximately 160 countries. Engineers are the straw that stirs medtechs drink (apologies to Reggie Jackson). Placement on the apophyseal ring helps prevent subsidence. Titan becomes the first to commercialize nanotechnology for the spine. 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. And functions implants micro and nano textures represent a significant advance in spine surgery is intended to long-term! 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Migration on microtextured titanium the merger Globus-Nuvasive 7/20/2015 separate Titan `` Urgent medical device Companies based on annual.., you will have a better Medtronic website experience Definitions if submitting registration results... ( apologies to Reggie Jackson ) clinical and radiological evidence of degenerative disc at... People worldwide, serving physicians, hospitals and patients in approximately 160 countries annual revenue not mean it been. & amp ; Bradstreet device that i have been using with great success titan endoskeleton tas surgical technique date and fusion the. Industry and RCTs people worldwide, serving physicians, hospitals and patients in approximately 160.! S.L., Slosar, P.J., Schneider, J.M., Schwartz, Z., Boyan, B.D,. A max of 15 clinical sites participate in a study rates of spinal implants.... Anatomical structures a robot or navigation system B., Riley, T., Platt, C., Brown J... 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