Next-generation occipito-cervico-thoracic fusion system features an advanced polyaxial screw for degenerative & complex spinal pathologies
Regulatory
Pentax Medical Europe Unveils Unique Duodenoscope with Disposable Elevator Cap
CE mark for Pentax Medical’s DEC™ Duodenoscope delivers clinicians a unique solution for enhancing infection prevention and improving reprocessing efficiency, says company
FDA Approval and U.S. Launch of Medtronic’s New Chronic Intractable Pain Platform
Intellis includes the world’s smallest implantable spinal cord stimulator
U.S. 510(K) Clearance for Adherium’s Smartinhaler for AstraZeneca’s Symbicort Aerosol
Data show improved adherence by up to 59% in adults and 180% in children
CE Mark and EU Launch of MyoVista® High Sensitivity ECG Device
Low-Cost cardiac screening advancement aims to improve early detection of heart disease
FDA Clears COALESCE™ Porous PEEK Lumbar Interbody Fusion Device
Material benefits said to include improved biologic fusion and biomechanics
FDA Clearance for “Game Changing” Cardiologs ECG Analysis Platform
Cloud-based “AI” cardiac monitoring-analysis web service gets U.S. go ahead
FDA Clearance and CE Mark for K2M NILE® Proximal Fixation Spinal System
Specifically designed for proximal construct augmentation, K2M says NILE provides versatile option to help achieve 3D spinal balance in complex spine procedures
FDA Approves VNS Epilepsy Therapy in Children as Young as Four
VNS Therapy becomes the first and only FDA approved device for pediatric drug-resistant epilepsy
Canada Approves Abbott’s Glucose Sensor
System offers freedom from finger sticking for diabetic community
K2M First-to-Market with 3D-Printed Corpectomy Cage System
FDA Clears CAPRI™ Small 3D Static featuring lamellar 3D Titanium Technology™
Spineology® Enters Anterior Fusion Market with Rampart One™ FDA Clearance
Rampart One brings anatomy-conserving design to ALIF, says Spineology
FDA Clearance and Launch of OrbusNeich Coronary Dilatation Catheters
Announcement marks company’s official entry into the US market
FDA Approval For Ethicon’s SURGICEL® Powder Absorbable Hemostat
Surgicel Powder targets control of continuous oozing on broad or raw surfaces
FDA Clears Claret Medical’s Sentinel Cerebral Protection System
First and only embolic protection device shown to reduce TAVR procedural strokes by 63 Percent
Indian Approval Opens up $3.5billion Market for Zip® Wound Closure System
And new clinical study demonstrates higher tissue perfusion than staple closure in Total Ankle Replacement Surgery