Implants

MicroVention Announces FDA Premarket Approval of a New Flow Diverter for the Treatment of Brain Aneurysms

MicroVention Announces FDA Premarket Approval of a New Flow Diverter for the Treatment of Brain Aneurysms

ALISO VIEJO, Calif., Jan. 9, 2020 /PRNewswire/ -- MicroVention, Inc., a U.S. based subsidiary of Terumo and a global neurovascular company announced the FDA Premarket Approval (PMA) for the FRED® (Flow Re-Direction Endoluminal Device) device for the treatment of brain aneurysms. The FRED® device is the first flow diverter in the U.S. to use a self-expanding braided nitinol mesh to help...

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New Porous Titanium Implant from NuVasive is Ideal for Cervical Applications

New Porous Titanium Implant from NuVasive is Ideal for Cervical Applications

Include Porous PEEK and porous titanium offerings for anterior cervical discectomy and fusion (ACDF) techniques. Modulus implants designed for bone in-growth, while mimicking a stiffness and allowing for enhanced visualization on a variety of imaging modalities. Designed to combine inherent benefits of porosity with the advantageous material properties of titanium.

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New AlphaGRAFT DBM Fiber Technology Improves Regenerative Capacity

New AlphaGRAFT DBM Fiber Technology Improves Regenerative Capacity

Optimized handling enables combination with allograft or autograft for use in spinal fusion procedures. Provides moldable allograft with cohesive handling characteristics and osteoconductive scaffold for delivery of autologous stem cells. Regenerative capacity exhibits all five elements of new bone formation in validated animal models.

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Centinel Presents STALIF L FLX Implant System with FUSE-THRU Trabecular Scaffold

Centinel Presents STALIF L FLX Implant System with FUSE-THRU Trabecular Scaffold

The STALIF L FLX Lateral Lumbar Integrated Implant System comes with combination of solid and porous radiolucent sections that reduce mechanical stiffness. The trabecular scaffold allows for bony in-growth throughout the implant. The system features No Profile® integrated compressive lag screws that are used at one or two contiguous levels with both autograft and/or allogenic bone graft.

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Edwards' SAPIEN 3 Ultra Transcatheter Heart Valve Receives FDA Approval

Edwards' SAPIEN 3 Ultra Transcatheter Heart Valve Receives FDA Approval

Irvine, Calif., Dec. 28, 2018 /PRNewswire/ -- Edwards Lifesciences Corporation (NYSE: EW), the global leader in patient-focused innovations for structural heart disease and critical care monitoring, today announced that the SAPIEN 3 Ultra system has received U.S. Food and Drug Administration (FDA) approval for transcatheter aortic valve replacement in severe, symptomatic aortic stenosis...

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New OVOMotion Shoulder Arthroplasty System by Anthrosurface Features Inlay Glenoid

New OVOMotion Shoulder Arthroplasty System by Anthrosurface Features Inlay Glenoid

Anthrosurface’s new OVOMotion system offers minimal bone removal and increased glenoid exposure via an added planar cut. Featuring an aspherical head design and improved joint access, the product is designed for patients with painful or severely disabled shoulder joints from arthritis, AVN, or traumatic events. The OVOMotion system also features more biomechanical stability than other shoulder...

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DynaFORCE-® Implant System meets FDA standards.

DynaFORCE-® Implant System meets FDA standards.

DynaFORCE® Active Stabilization™ Vero Medial Column Implant System is offered in different sizes and completely sterile packed for delivery. This system combines the stability of a plate with active compression of nitinol clips and allows surgeons to address compression across multiple joints.

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