The US Food and Drug Administration approvedAbbott’s Aveir dual chamber (DR) leadless pacemaker system.
About 80% of people who need a pacemaker to treat bradycardia or another abnormal heart rhythm will need dual-chamber...
Cardio Catch-Up: Abbott Plans To Expand Pacemaker Market With Leadless Aveir DR
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The FDA approved Abbott’s Aveir DR dual-chamber leadless pacemaker system, which will complement Abbott’s Aveir VR technology and help Abbott compete directly with Medtronic in the growing leadless cardiac rhythm management device market.
Keep up with the top medtech business and regulatory news.
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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.
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