A manual compression assist product, t he original Cardiva Boomerang Wire vascular closure device received FDA clearance in 2004. The next generation technology, Cardiva Catalyst II achieved FDA approval in 2007 and the device is also is CE Marked for distribution in Europe. According...
read full descriptionCaReS (Cartilage Regeneration System) is a patented collagen type 1 matrix colonised with autologous cartilage cells for use in the repair of articular surface defects. CaReS-OneStep is a cell-free matrix.
read full descriptionAccording to the manufacturer, this closed-cell low-profile device is designed to provide tracking through tortuous anatomy. The monorail delivery system allows rapid catheter exchanges. They say that the Carotid Wallstent is the only carotid stent indicated for use in high...
read full descriptionThe Cartilage Autograft Implantation System (CAIS) is a single surgery system for cartilage repair developed by Depuy Mitek and Johnson and Johnson Regenerative Therapeutics. The scaffold implant is a resorbable copolymer foam, attached with resorbable PDS staples. Ongoing clinical trials can...
read full descriptionThe CARTO 3 System is the next generation magnetic tracking 3D mapping system from Biosense Webster, building on the accuracy of CARTO System magnetic navigation technology. Notes In February 2012, the MHRA issued a field safety notice for this device. Find out more here .
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