Tag: Medtronic
Philips and Medtronic partner to help accelerate access to life-saving stroke...
Royal Philips and Medtronic Neurovascular today announced a strategic advocacy partnership that will see the two companies attempt to raise awareness around potential health...
Axonics prevails in patent infringement lawsuit with Medtronic
Axonics has announced that the jury has returned a unanimous verdict in the patent infringement lawsuit brought by Medtronic against the company in US...
Medtronic receives “landmark” US FDA approval for asleep deep brain stimulation...
Medtronic has received US Food and Drug Administration (FDA) approval of asleep deep brain stimulation (DBS) surgery for people with Parkinson’s disease and people...
Medtronic unveils next-generation Artisse intrasaccular device alongside new data at LINNC...
Medtronic has today announced the European launch of Artisse—a new intrasaccular device designed to treat intracranial aneurysms by conforming to the shape of the...
Conformability, softness, simplicity and simulation enable Artisse to ‘personalise’ treatments in...
This advertorial, intended for readers outside the USA only, is sponsored by Medtronic.
In light of the official European launch of the Artisse aneurysm embolisation...
Medtronic names Linnea Burman as new head of Neurovascular business
Medtronic has today announced that Linnea Burman will succeed Dan Volz as its senior vice president (SVP) and president of its Neurovascular business—part of...
Dedicated devices support progress towards “next frontier” for stroke thrombectomy
This advertorial, intended for readers outside the USA only, is sponsored by Medtronic.
In light of a recent publication detailing the safe and effective use...
Research, training and industry all key to better thrombectomy care in...
This advertorial is sponsored by Medtronic.
Late last year, on 24 November, a decade’s work from a passionate group of physicians bore fruit, with the...
Viz.ai and Medtronic to collaborate on improving post-cryptogenic stroke care in...
Viz.ai has announced a strategic collaboration with Medtronic to improve the coordination of cryptogenic stroke patient care between neurology and cardiology teams.
For stroke patients...
US patent office rejects Axonics’ latest challenge to Medtronic patents
Medtronic has announced that the Patent Trial and Appeal Board (PTAB) of the US Patent and Trademark Office has affirmed the validity of claims...
Medtronic files complaint against Axonics to stop “unauthorised use” of neuromodulation...
Medtronic recently announced that it has filed a complaint with the US International Trade Commission (ITC), along with a parallel action in US District...
Medtronic announces first neurointerventional case with CE-marked Rist 6Fr radial access...
Medtronic has announced the first neurointerventional case in Europe with its Rist 6Fr radial access catheter, which recently received regulatory approval for use in...
Medtronic announces trial data on closed-loop and DTM SCS therapies at...
At this year’s North American Neuromodulation Society (NANS) annual meeting (18–21 January, Las Vegas, USA), Medtronic announced new data from two clinical trials demonstrating...
Medtronic gains US FDA approval for Percept RC deep brain stimulation...
Medtronic has announced the US Food and Drug Administration (FDA) approval of its Percept RC deep brain stimulation (DBS) system.
The rechargeable neurostimulator is the...
Newly published PROST trial results find Preset non-inferior to Solitaire in...
Final results from the PROST randomised controlled trial (RCT) have been published in JAMA Neurology and—according to the study’s leading investigators—provide evidence that thrombectomy...
INSPIRE-S registry offers comprehensive, real-world data on acute ischaemic stroke devices
This advertorial is sponsored by Medtronic.
As part of the company’s ongoing commitment to offering physicians access to high-quality clinical data and, subsequently, enabling evidence-based...
APRO catheters offer ‘gold-standard’ trackability with robustness and stent-retriever compatibility to...
This advertorial is sponsored by Medtronic.
As the co-founder and chief executive officer of Chestnut Medical, Aaron Berez played a leading role in bringing flow...
INSPIRE-A registry helps pave way for standardised assessment of flow-diverter imaging...
This advertorial is sponsored by Medtronic.
As a prospective, independently adjudicated registry boasting a highly comprehensive patient dataset, INSPIRE-A is a “very unique” phenomenon in...
Medtronic names Paolo Di Vincenzo president of its neuromodulation business
Medtronic has shared that Paolo Di Vincenzo will join the company as president of its neuromodulation business, effective 30 October 2023. In this role,...
Old but still gold—why coiling remains a vital tool for treating...
This advertorial is sponsored by Medtronic.
Alberto Nania (National Health Service Lothian, Edinburgh, UK) speaks to NeuroNews to outline how, despite the rapid proliferation...
Medtronic receives CE-mark approval for Inceptiv closed-loop SCS to treat chronic...
Medtronic has received CE-mark approval for its Inceptiv closed-loop rechargeable spinal cord stimulator in the treatment of chronic pain.
Inceptiv is the first Medtronic spinal...
Medtronic to highlight sensing-enabled spinal cord stimulation research at NANS 2023
Medtronic has announced that it will highlight clinical and preclinical research relating to sensing-enabled spinal cord stimulation (SCS) therapy at the North American Neuromodulation...
Medtronic Neurovascular partners with Avail to boost real-time connectivity
Medtronic Neurovascular has announced a new partnership with Avail Medsystems, creating the Medtronic Remote Connectivity Program (Medtronic RCP) in the process.
The goal of this...
SWIFT DIRECT does not show statistical non-inferiority of direct mechanical thrombectomy...
NOTE: This video is ONLY available to watch in selected countries and geographies
Principal investigators Urs Fischer (University Hospital of Basel, Basel, Switzerland) and...
IRRAS announces commercial US partnership with Medtronic for IRRAflow system
IRRAS recently announced it has signed a sales agency agreement to promote its IRRAflow system in the USA with Medtronic.
During the initial pilot phase of this...
Medtronic study finds post-stroke protocols “vary significantly” between community hospitals and...
Medtronic has announced the first results from its DiVERT clinical study, which showed that post-stroke workflow protocols and cardiac monitoring vary significantly across community...
Medtronic announces launch of neurovascular Co-Lab platform
Medtronic has announced the launch of its neurovascular Co-Lab platform, which is designed to accelerate "urgently needed" innovation in stroke care and treatment.
The company...
Similar complication rates observed following DAPT discontinuation within and past 90...
The duration of dual antiplatelet therapy (DAPT), either 30–90 days or more than 90 days, following implantation of a flow diverter in cerebral aneurysm...
It takes two: The benefits of direct ‘double stentriever’ thrombectomy in...
This advertorial, sponsored by Medtronic, is intended for readers outside of the USA.
Mechanical thrombectomy may be the standard of care for acute ischaemic strokes...
Medtronic announces first implant in study evaluating investigational, closed-loop neurostimulator
Medtronic today announced the first patient implant in a clinical study of its investigative, closed-loop, implantable neurostimulator. The ‘Evaluation of long-term patient experience with...
Medtronic names Laura Mauri as new chief scientific, medical and regulatory...
Medtronic has announced that Laura Mauri has been appointed as the company’s chief scientific, medical and regulatory officer. This appointment adds to Mauri's prior responsibilities...
Radial access is not just a new toy—it has come to...
This advertorial is sponsored by Medtronic.
Upon gaining CE-mark approval in September of last year, the Rist radial access system (Medtronic) became the first dedicated...
Survey uncovers “far-reaching” impact of pandemic on patients with chronic back...
A new survey commissioned by Medtronic and conducted by public opinion research firm The Harris Poll has found that 44% of current chronic back...
Medtronic announces first patient implants of investigational TNM therapy for bladder...
Medtronic recently announced the first patients have been implanted in the TITAN 2 pivotal study—which will evaluate the safety and efficacy of its investigational...
Medtronic receives FDA approval for InterStim X system for bladder and...
Medtronic has announced receipt of approval from the US Food and Drug Administration (FDA) for its new, recharge-free InterStim system—with the device being made...
Medtronic announces FDA approval of SCS therapy for diabetic peripheral neuropathy
Medtronic has received US Food and Drug Administration (FDA) approval of its Intellis rechargeable neurostimulator and Vanta recharge-free neurostimulator for the treatment of chronic...
Medtronic announces results showing meaningful pain relief using DTM SCS endurance...
Medtronic has announced three-month results from an on-label, prospective, multicentre study showing meaningful pain relief using DTM SCS endurance therapy—a modified, lower-energy variation of the...
Medtronic announces schedule for sponsored presentations at NANS 2022
Medtronic has announced its schedule for presentations at the 25th North American Neuromodulation Society (NANS) annual meeting (13–15 January 2022; Orlando, USA). According to a press...
Antibiotic envelopes appear safe and effective in decreasing SCS surgical site...
Antibiotic impregnated envelopes appear to be a safe and effective modality for decreasing surgical site infection risks in spinal cord stimulation (SCS) implantation, according...
Rune Labs and Medtronic partner to improve understanding of neurostimulation with...
Rune Labs, a company using aggregated brain data to empower the development and delivery of precision medicines for neurological and psychiatric diseases, and global healthcare...
Study highlights temporal relationship between atrial fibrillation and stroke
Medtronic has announced the publication of a study demonstrating, through the use of a continuous rhythm monitoring device, that atrial fibrillation (AF) is directly...
Medtronic receives CE mark approval for radial artery access portfolio
Medtronic today announced it has received CE mark approval for its radial artery access portfolio, which includes the Rist radial access selective catheter and the Rist...
Medtronic recalls Pipeline Flex embolisation devices over risk of delivery system...
Medtronic has issued a recall of its Pipeline Flex embolisation device and Pipeline Flex embolisation device with Shield technology products due to a risk...
“Welcome and exciting”: Evidence mounts in favour of flow diversion technologies
Multiple pieces of clinical research supporting the use of flow diverter devices to treat intracranial aneurysms have come to light so far in 2021....
Direct mechanical thrombectomy fails to show non-inferiority compared with IV t-PA...
The preliminary results of the SWIFT-DIRECT (Solitaire with the intention for thrombectomy plus IV t-PA versus direct Solitaire stent-retriever thrombectomy in acute anterior circulation...
DTM SCS: A unique, tailored and highly effective therapy option for...
Michael Fishman (Wilmington, USA) discusses the benefits of Differential Target Multiplexed spinal cord stimulation (DTM SCS; Medtronic)—when compared to more conventional SCS therapy options—and...
Neurosurgery with Surgical Theater’s VR and AR technologies set for first...
Rambam Healthcare Medical Center in Haifa, Israel is set to become the first medical centre in Israel to use virtual reality (VR) and augmented...
Data from 1,000 aneurysms indicate Pipeline Embolization Device is safe and...
The endovascular treatment of intracranial aneurysms using the Pipeline Embolization Device (PED; Medtronic) has been deemed safe and effective following a study involving data...
Medtronic announces FDA approval of recharge-free Vanta spinal cord stimulation implant
Medtronic has received US Food and Drug Administration (FDA) approval for Vanta—a high-performance, recharge-free implantable neurostimulator (INS) with a device life that can be...
Livestreamed procedures close distance between clinicians and trainees during pandemic
Phil Taussky outlines a simple yet effective livestreaming platform that holds benefits for neurosurgeons during the ongoing COVID-19 crisis.
One of the challenges faced by...
Medtronic, Viz.ai partner to bring “lifesaving” AI platform for stroke to...
Medtronic and Viz.ai have announced they are extending their successful US partnership to distribute Viz.ai’s "lifesaving" artificial intelligence (AI) software platform for stroke to...
Medtronic and Surgical Theater to provide first real-time AR platform for...
Medtronic will partner with American health technology firm Surgical Theater to provide the first augmented reality (AR) platform for use in real time during...
Medtronic gains FDA approval to trial implantable tibial neuromodulation device
Medtronic has announced approval from the US Food and Drug Administration (FDA) to proceed with an investigational device exemption (IDE) trial to evaluate its...
FDA approves Medtronic Pipeline Flex with Shield Technology to treat brain...
Medtronic has received US Food and Drug Administration (FDA) approval for the Pipeline Flex embolization device with Shield Technology for the treatment of aneurysms.
Medtronic’s...
Medtronic receives CE mark for SenSight directional lead system for DBS...
Medtronic has announced that it has received CE mark for the SenSight directional lead system for deep brain stimulation (DBS) therapy as treatment of...
Medtronic announces release of its new radial artery access portfolio
Medtronic today announced expansion of the limited site release of its recently acquired radial artery access portfolio from privately-held Rist Neurovascular, following first-in-patient procedure....
Medtronic launches aDBS trial in Parkinson’s disease patients
Medtronic has announced the first enrolment in its trial evaluating the safety and efficacy of adaptive deep brain stimulation (aDBS) in patients with Parkinson’s...
Medtronic announces first patient implanted in study (ELITE) of InterStim Micro
Medtronic has announced it has been implanted the first patient in its evaluation of InterStim Micro system performance and safety (ELITE) study of the...
Medtronic announces US launch of its InterStim Micro neurostimulator
Medtronic has announced that its recently US Food and Drug Administration (FDA)-approved InterStim Micro neurostimulator for sacral neuromodulation (SNM) therapy is now available in...
FDA approves Percept PC neurostimulator with BrainSense technology
Medtronic has announced it received US Food and Drug Administration (FDA) approval for the Percept PC deep brain stimulation (DBS) system. BrainSense technology makes...
Medtronic provides ventilator progress update
Medtronic has announced updates regarding its efforts to increase ventilator production around the globe. The company is announcing progress in the ramp-up of its...
Medtronic shares ventilation design specifications to accelerate efforts to increase global...
Medtronic has announced it is publicly sharing the design specifications for the Puritan Bennett 560 (PB 560) to enable participants across industries to evaluate...
Medtronic issues urgent field safety notice for some Pipeline Flex embolisation...
Medtronic has issued an urgent field safety notice to warn on specific production lots of its Pipeline Flex embolisation devices due to the potential...
Medtronic launches Efficio software to help clinicians efficiently manage targeted drug...
Medtronic announce the launch of Efficio, a cloud-based data management software for use with the SynchroMed II intrathecal drug delivery system, that will allow...
DTM spinal cord stimulation using Medtronic’s Intellis platform shows superior back...
Three-month results from a large, multicentre randomised controlled trial (RCT) has demonstrated statistically significant (p=0.0009) and superior back pain relief with differential target multiplexed...
Medtronic acquires Stimgenics, pioneer of Differential Target Multiplexed spinal cord stimulation
Medtronic has acquired Stimgenics, a privately-held company that has pioneered a novel spinal cord stimulation (SCS) waveform known as Differential Target Multiplexed (DTM) Spinal...
Medtronic announces FDA submission for InterStim Micro neurostimulator and SureScanTM MRI...
Medtronic announces it has filed a premarket approval (PMA) supplement with the US Food and Drug Administration (FDA) for approval of its InterStim Micro...
Omar Ishrak to step down as Medtronic CEO next year
Omar Ishrak, Medtronic’s chairman and CEO is to retire on 26 April 2020, following the end of the company’s current fiscal year. Also, the...
Medtronic’s Evolve workflow with spinal cord stimulation demonstrates effective pain relief...
Medtronic has announced primary endpoint (three-month) results of the Vectors post-market clinical study that demonstrated effective pain relief and improved function in patients with...
Medtronic announces FDA clearance and US launch of the Accurian RF...
Medtronic has announced US Food and Drug Administration (FDA) 510(k) clearance of the Accurian RF ablation platform, which conducts radio frequency (RF) ablation of...
Medtronic’s deep brain stimulation for medically-refractory epilepsy launches in the USA
Medtronic has announced both the US launch of deep brain stimulation (DBS) for medically-refractory epilepsy and the first commercially implanted patient at Emory University...
FDA approval on expanded indication for Pipeline Flex embolisation device
Medtronic has announced that it has received US Food and Drug Administration (FDA) approval on an expanded indication for its Pipeline Flex embolisation device. Previously...
Acute ischaemic stroke care continuum: With stroke patients every step of...
This video has been sponsored by Medtronic
With the treatment paradigm for stroke still evolving and the community committed to discovering and implementing the most...
Acute ischaemic stroke care continuum: With stroke patients every step of...
The fact that endovascular therapy is now well established for patients with acute ischaemic stroke has changed the face of stroke treatment forever. The last five...
First patient enrolled in Embrace targeted drug delivery clinical study
The first patient has been enrolled in the Embrace TDD (targeted drug delivery) clinical study that will evaluate the use of the SynchroMed II...
FDA approves new SynchroMed II myPTM Personal Therapy Manager that enables...
Medtronic has announced US Food and Drug Administration (FDA) approval of the new SynchroMed II myPTM Personal Therapy Manager for patients with chronic pain....
Medtronic launches the Control Workflow to help eliminate oral opioids and...
Medtronic has announced the US launch of the Control Workflow, an evidence-based approach for use with the SynchroMed II intrathecal drug delivery system ("Medtronic...
New clinician programmer for deep brain stimulation therapy
The US Food and Drug Administration (FDA) has recently approved Medtronic’s state-of-the art Deep Brain Stimulation (DBS) Clinician Programmer and Activa Programming Application, which...
Medtronic receives FDA Approval for deep brain stimulation therapy for medically...
The US Food and Drug Administration (FDA) has granted premarket approval for Medtronic's deep brain stimulation (DBS) therapy as adjunctive treatment for reducing the...
To By-Pass or Not To By-Pass
In this educational supplement we focus on ischaemic stroke. We look at the results of the ASTER trial and experts weigh in on the...
Medtronic gets US FDA clearance for Riptide aspiration system
The Riptide aspiration system is intended for use in the revascularisation of patients with acute ischaemic stroke secondary to intracranial large vessel occlusive disease...
FDA approves new clinician programmer for SynchroMed II intrathecal drug delivery...
The US Food and Drug Administration (FDA) has approved a new clinician programmer for use with the SynchroMed II Intrathecal Drug Delivery system (Medtronic),...
First patient enrolled in study to assess optimised spinal cord stimulation...
The first patient has been enrolled in the Vectors Post Market Clinical Study. The study will follow patients with chronic intractable pain who are...
Intellis platform receives CE mark for spinal cord and peripheral nerve...
Medtronic has received CE mark for the Intellis platform for both spinal cord stimulation (SCS) and peripheral nerve stimulation (PNS) as an aid in...
FDA approves Intellis platform for chronic pain
The US Food and Drug Administration has approved the Intellis spinal cord stimulation platform (Medtronic) for the management of certain types of chronic intractable...
SureTune3 earns CE mark for deep brain stimulation therapy
CE mark has been granted to the SureTune3 software (Medtronic) for deep brain stimulation (DBS). SureTune3 provides patient-specific visualisation of lead location and simulated...
SureTune3 deep brain stimulation software receives Health Canada licence
Medtronic has received a Health Canada licence for SureTune3 software for deep brain stimulation (DBS). The latest innovations in the SureTune technology are designed...
Medtronic announces voluntary worldwide recall of its StrataMR adjustable valves and...
Medtronic has announced that on 22 February, 2017 it notified customers of a voluntary recall of all unused units of the StrataMR adjustable valves...
Better neck coverage with “bulged centre” of Barrel device in wide-necked...
A single-centre study reports that stent-assisted coiling with the Barrel stent (Medtronic) is a feasible, safe, and efficient method for embolisation of intracranial wide-necked...
FDA clears Reveal LINQ Insertable Cardiac Monitor with TruRhythm Detection
The US Food and Drug Administration (FDA) has given 510(k) clearance to Medtronic for its Reveal LINQ Insertable Cardiac Monitor (ICM) with TruRhythm Detection.
A...
Medina embolisation device represents “a major step forward” in aneurysm treatment
According to a report of a single centre’s experience using the Medina embolisation device (Medtronic) for the treatment of unruptured aneurysms, the device “represents...
Introducing the new Solitaire™ Platinum Revascularization Device
The Solitaire™ Platinum Revascularization Device is the next generation into the Solitaire™ family which has an enhanced meaningful visibility that provides feedback during placement,...
FDA expands indication of Solitaire device
The US Food and Drug Administration (FDA) has cleared an expanded indication for the Solitaire stent retriever device (Medtronic). The FDA now allows the...
Medtronic announces voluntary recall of its Pipeline embolization device, Alligator retrieval...
Medtronic has announced that it has notified customers of a voluntary recall of certain lots of its Pipeline embolization device, Alligator retrieval device and...
Medtronic’s StealthStation cranial software receives FDA clearance as an aid for...
Medtronic has announced US Food and Drug Administration (FDA) clearance of StealthStation cranial software as an aid for deep brain stimulation (DBS) lead placement....
CE mark granted to Medtronic for SureTune2 deep brain stimulation therapy
Medtronic has received CE mark for SureTune2 software, which is designed to provide patient-specific visualisation to help physicians make decisions on how to program...
Medina Embolization Device and Pipeline Shield: LINNC Wrap Up Interviews
Find the latest updates from Prof Monika Killer and Dr Saleh Lamin following this year’s LINNC Congress in Paris. We consider our latest technologies,...
World Stroke Organisation and Medtronic to promote stroke awareness
The World Stroke Organization has announced a global partnership with Medtronic to increase stroke awareness through several initiatives.
The two organisations will work together with...
Medina Embolization Device
Medina™ is designed as an intra-saccular flow diverter, diverting flow away from the aneurysm sac and through the parent artery by forming a mesh scaffold...
Medtronic offer first complete portfolio of full-body MR conditional neurostimulation systems
The US Food and Drug Administration (FDA) has approved Medtronic’s Specify SureScan MRI surgical leads, which are indicated for use as part of Medtronic...
High-density stimulation restores efficacy in failed spinal cord stimulation therapy
By reprogramming existing spinal cord stimulation systems, investigators have been able to restore efficacy in patients who have failed spinal cord stimulation therapy, and...
Almost no learning curve with Barrel reconstruction device
The Barrel Vascular Reconstruction device (Medtronic) is one of the newest offerings for the treatment of intracranial bifurcation aneurysms. Since receiving the CE mark...
Medtronic and Samsung to collaborate on telehealth solutions for neuromodulation patients
Medtronic and Samsung Electronics America are to begin a broad-based strategic alliance aiming to speed up the development of digital health solutions for those...
Stent retriever technology named as a Top Medical Innovation by Cleveland...
Stent retriever technology has been named by the Cleveland Clinic as a top medical innovation. It was part of a list of the top...
Medtronic TYRX Neuro Absorbable Antibacterial Envelope now available for use with...
Medtronic plc has announced the first implants of the TYRX Absorbable Antibacterial Envelope with Medtronic deep brain stimulation (DBS) systems. The implants were conducted...
Medtronic acquires Lazarus Effect
Medtronic plc has announced that it has acquired Lazarus Effect, a Campbell, California, USA-based and privately-held medical device company focused on acute ischaemic stroke...
Medtronic launches Arc support catheter series in USA for treatment of...
Medtronic plc has announced the US launch of the Arc support catheter, the most navigable, 6F tapered support catheter available. Developed to improve delivery of...
Medtronic acquires Medina Medical
Medtronic plc has announced that it has acquired Medina Medical, a Menlo Park, California, USA-based and privately-held medical device company focused on commercialising state-of-the-art...
Radiation reduced with flow diversion for treatment of internal carotid artery...
According to new research, treatment of large and giant proximal internal carotid artery aneurysms using the Pipeline embolisation device (Covidien/Medtronic) requires less radiation, less...
Medtronic announces European approval of the first and only full-body MR...
The expanded approval for full-body MRI scans applies to all patients receiving a new system and to an estimated 13,000 people in Europe already receiving Medtronic DBS therapy.
Evidence builds for endovascular treatment of acute ischaemic stroke
With the publication of two more stroke trials, the evidence in favour of endovascular treatment in patients with acute ischaemic stroke has reached new heights. Data from SWIFT PRIME and REVASCAT add to that of three other trials-MR CLEAN, EXTEND-IA and ESCAPE-that have begun to change the face of ischaemic stroke treatment.
Next generation Medina coil system shows improvements in early human experience
In early use of the Medina coil system, researchers have found the device to be a next generation coil that combines the familiar procedural safety and technique associated with conventional coils, with improved circumferential aneurysm filling, which, they say, it is thought will lead to improved long-term outcomes.
Groundbreaking studies find that neurointerventional surgery reduces stroke mortality
Two new clinical trials on the treatment of stroke (ESCAPE and EXTEND IA) demonstrate that neurointerventional surgery significantly increases the number of patients who are able to live independently without major neurological disabilities.
FDA approves Pipeline Flex embolisation device
Designed to divert blood flow away from an aneurysm, the Pipeline Flex embolisation device (Medtronic) features a braided cylindrical mesh tube that is implanted across the base or neck of the aneurysm.