Specifically designed for proximal construct augmentation, K2M says NILE provides versatile option to help achieve 3D spinal balance in complex spine procedures
Approval/Clearance
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
Abbott Says Newly CE Marked Confirm Rx™ ICM Represents New Paradigm
Device automatically captures vital cardiac information and relays data to physicians via smartphone app, enabling remote monitoring of irregular hearth rhythms
FDA Clears Teleflex Arrow® AC3 Optimus™ Intra-Aortic Balloon Pump
Teleflex claims advanced IABP performance with the ability to provide optimized therapy to the most challenging patient conditions
Samsung Launches New Ultrasound Systems
Designed to enhance the user experience, Samsung’s HS50 and HS60 bring the image quality and advanced technologies from their high-end systems to a mid-range price point, says company
FDA Nod for Paxman’s Scalp Cooler
Company to offer patients novel pay-as-you-go scheme as it aims to revolutionize U.S. scalp-cooling landscape
U.S. FDA Clearance For UOC’s Polyethylene Knee Insert
Knee insert is designed to provide patients with knee replacements with reduced risk of oxidation
CE Mark for REVA’s Fantom Drug-Eluting Bioresorbable Stent
European launch of Fantom coronary stent underway
FDA Clearance for “Procedure in a Box” Uni Knee System
Bodycad receives FDA 510K clearance for personalized unicompartmental knee system