The US FDA approved Boston Scientific's Lotus Edge transcatheter aortic valve for patients who would be at high risk with surgical valve replacement. Unlike competing TAVR systems from Medtronic and Edwards, Lotus Edge can be repositioned or recaptured after it has been deployed.
• Source: shutterstock.com
Boston Scientific Corp. immediately began a limited US launch of its Lotus Edge mechanically expanded transcatheter aortic valve replacement (TAVR) system after the US Food & Drug Administration approved it on 23 April.
Lotus Edge will compete with Edwards Lifesciences Corp.'s Sapien 3 balloon-expandable valve and Medtronic’s CoreValve Evaluate R self-expanding valve...
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Children with biliary atresia (BA) exhibited neurodevelopmental deficits and increased autism traits, with earlier surgery linked to better general neurodevelopment.
This week, Establishment Labs Holdings announced the FDA gave it premarket approval for Motiva breast implant, Cologuard lands FDA approval for Cologuard Plus and GE HealthCare gets FDA nod for a new imaging agent. The FDA announces another expansion for TAP into ophthalmology and radiology. The AAMI and CTA will join forces to develop standards for AI and ML-enabled health care products.
Children with biliary atresia (BA) exhibited neurodevelopmental deficits and increased autism traits, with earlier surgery linked to better general neurodevelopment.