UK vascular device specialist Veryan Medical has developed a stent design technology which aims to mimic the helical shape of peripheral vessels in the hope that this will have a vasoprotective effect and furthermore reduce risk of deformation and vessel trauma during leg flexion.
Vascular
FDA Approval Means Zilver® PTX® Is First Drug-Eluting PAD Stent In U.S.
Peripheral vascular disease treatments have shuffled under the spotlight in recent months with a seemingly endless trail of new devices and approvals for unblocking diseased vasculature. Now Cook Medical can say it has the first drug-eluting stent to be FDA approved for the job.
Biotronik’s Pulsar 18 IDE Study Gets First U.S. Patient
More good news for Biotronik’s peripheral vascular business as its Pulsar 18 study gets underway in the U.S., hot on the heels of favourable clinical study results from Europe.
Biotronik Pulsar SFA Stent Study Suggests It’s Just As Good With Heavily Calcified Lesions
Clinical study results show strong evidence of benefits for lower limb intervention when using Pulsar stents, with no statistical difference between heavily calcified and non calcified lesions.
Ovation Stent Graft PMA Means Small Femoral Arteries No Longer A Barrier To EVAR
Just over two years after it was CE marked, TriVascular’s Ovation Stent Graft, suitable for use in patients with small vascular access and challenging anatomy, has gained full approval in the United States.
New Approval Means Cordis Has First Stent In The U.S. With SFA And Iliac Indications
J&J subsidiary, Cordis Corporation has announced that the U.S. FDA has approved its S.M.A.R.T.® CONTROL® Vascular Stent Systems for use in the superficial femoral artery and/or the proximal popliteal artery.
Boston Buys Vessix… Like Night Follows Day
Well well well. All the big players have renal denervation systems in development or already in the catalogue. Now, so does Boston Scientific with the year’s least surprising acquisition of Vessix Vascular.
Study Says St.Jude’s EnligHTN Renal Denervation Technology Is Safe And Effective At Six Months
Data from the St.Jude EnligHTN I multi-electrode renal denervation catheter study presented at the annual scientific meeting of the American Heart Association suggests blood pressure reduction is sustained at six months.
New Report Says Obesity In Middle East Will Drive Vascular Device Growth
U.S. market intelligence company Millennium Research Group has issued a new report into vascular disease trends in the Middle East and reckons obesity is a key driver for future vascular therapies in the region. Dunno why but I have an image of a supersized
American wagging his finger at a well-built Arab and calling him fat.
CE Mark For Blue Medical’s Protégé NC Non Compliant, High Pressure, Drug Eluting Balloon
Blue Medical, the global medical device company and innovator in the treatment of vascular diseases, today announced receiving the CE mark for Protégé NC, a non compliant drug eluting balloon.
More Patients, More Good News For Renal Denervation In Medtronic Symplicity™ Study
New Data Presented at the 24th Annual Transcatheter Cardiovascular Therapeutics Scientific Symposium Show Sustained Blood Pressure Reduction and Safety with Symplicity™ Renal Denervation System in Patients with Treatment-Resistant Hypertension
Cardionovum® Says Clinical Support Is Fuelling Rapid Commercialisation Of Its Drug Coated Balloons
German company Cardionovum GmbH has updated us with the news that its distribution network, covering 57 countries, is pressing ahead with the commercialisation of its Primus® paclitaxel-coated balloon based on preclinical and clinical support.
Aorfix™ AAA Stent Graft Progressing Towards PMA To Include Patients With Tortuous Anatomy
Lombard Medical Technologies PLC, is confident it will jump the final hurdles as it gains written feedback from the U.S. FDA on the PMA application for Aorfix™, the Company’s flexible stent graft for the endovascular repair of abdominal aortic aneurysms.
Torqueability, Pushability, Steerability Key Words For Boston Sci’s New Victory™ PAD Guidewire
Boston Scientific Corporation has announced the U.S. and European launch of its Victory™ guidewire, designed to facilitate crossing of resistant lesions and the placement and exchange of balloon catheters or other interventional devices within the peripheral vasculature.
PAD Study Hints At Benefits Of 3D Stent Technology At 12 Months
Clinical study results presented this week are being touted as support for the theory that by inducing a three dimensional component into a mechanical stent, its flow characteristics will mimic the natural geometry of human vessels.
Results From Covidien’s Peripheral Arterial Disease Study Point To Effectiveness Of Atherectomy
Study confirms effectiveness of directional Atherectomy with SilverHawk ™ and TurboHawk ™ Devices as a frontline therapy when treating PAD