The new approval allows Medtronic to promote cryoablation as the first option for patients with recurrent symptomatic paroxysmal atrial fibrillation. Previously, it was only approved for patients who had already tried to manage their atrial fibrillation with drugs.
MEDTRONIC'S ARCTIC FRONT ADVANCE CRYOBALLOON • Source: Medtronic PLC
Medtronic plc’s Arctic Front cardiac cryoablation system is the first cardiac ablation device approved by the US Food and Drug Administration for “first-line” treatment of symptomatic paroxysmal (occasional) atrial fibrillation, the agency announced on 21 June.
The FDA approved a PMA supplement to expand Arctic Front’s indications to include the treatment of recurrent symptomatic paroxysmal...
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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.