Gore-designed all-in-one system to preserve iliac artery blood flow in patients with iliac or aortoiliac aneurysms
Regulatory
CE Mark for Medtronic’s Full Line of MRI Compatible CRT-Ds
Medtonic is now able to offer both 1.5 and 3 Tesla indications for MR-Conditional ICMs, Pacemakers, ICDs and CRT-Ds
FDA Approval for St . Jude’s “Industry First” MultiPoint Pacing Technology
Quadra Assura MP™ CRT-D, Quadra Allure MP™ CRT-P and additional Quartet™ LV lead options broaden the St. Jude Medical industry-leading heart failure portfolio in the U.S.
FDA Approval for LivaNova’s CROWN PRT™ Stented Heart Valve
Sorin/Cyberonics coming together as LivaNova followed by two valve approvals
CE Mark for K2M’s Next-Generation Cervical Disc System
RHINE™ Cervical Disc System boasts proprietary molding technology to minimize wear between polymer core and metal endplates
Medtronic Says Newly Acquired OsteoCool™ RF Ablation System Now FDA Cleared
Cooled RF Ablation system targets pain reduction in resection of spinal metastases
FDA Approval for Perceval Sutureless Heart Valve
Major milestone as patients needing open aortic valve replacement benefit from easier-to-implant prosthesis
FDA Clears NeuroMetrix Next Generation Quell® Wearable Pain Relief Technology
New clearance for use of Quell Relief smartphone app provides unprecedented level of convenience and comfort when usi treat chronic pain
Maquet Launches New Ventilation Solutions for Critical Care Hospital Settings
Maquet Medical Systems USA has now officially launched two new intensive care ventilators, SERVO-U®, and its dedicated neonatal intensive care solution, SERVO-n®
World’s First Spinal Fusion Surgery with Guided Pedicle Screws
“Direct insertion of pedicle screws along with real-time x-ray-free feedback represents a key step for spine surgery”
FDA Clears Life Spine® GRUVE™ Anterior Cervical Plate System
Spinal device company Life Spine, has gained U.S. FDA 510(k) marketing clearance for its GRUVE Anterior Cervical Plate System.
Moximed® Springs Forward with CE Mark of Atlas™ Knee System
Shock absorber for the knee sees first commercial use following regulatory approval
CE Mark for Mynosys ZEPTO Capsulotomy Device
Device promises 360 degree simultaneous capsulotomy in milliseconds
FDA Approval And CE Mark for Boston Scientific’s DVT Catheter
ZelanteDVT catheter is the first AngioJet catheter designed specifically to treat DVT
CE mark for Xenios® i-cor® Synchronized Cardiac Assist System
Clever idea comes to fruition as i-cor Syncronized Cardiac Assist device gains European clearance
FDA Approves St. Jude’s New User-Friendly Chronic Pain System
Patient-centric, recharge-free, upgradeable, MR-conditional, the Proclaim™ Elite SCS System targets patients’ quality of life