News Daily News Direct Delivery of Antibiotics to CV Device Pocket Infections Appears Promising Todd Neale January 09, 2023
News Conference News HRS 2022 Fewer Lead-Related Complications With Subcutaneous ICD: ATLAS S-ICD Todd Neale April 30, 2022
News Daily News The NCDR Has Made a Difference, but Experts See Room for Growth Todd Neale April 28, 2022
News Conference News ACC 2022 Most Infected Cardiac Implanted Electronic Devices Not Removed Fast Enough Michael O'Riordan April 04, 2022
News Features Roughly 80% of ESC Guideline Writers Have Financial COIs Michael O'Riordan April 01, 2021
News Daily News Safe to Upgrade From Pacemaker or Defibrillator to CRT Michael O'Riordan February 10, 2021
News Daily News Smartphones and Watches Unlikely to Interfere With Implanted CV Devices Yael L. Maxwell August 05, 2020
News Daily News Tricuspid Interventions OK With Pacemakers, ICDs: TriValve Registry Todd Neale January 17, 2020
News Daily News Year in Review: Digital Health and A-fib Ablation Top 2019 Heart Rhythm News Todd Neale December 19, 2019
News Daily News Safe to Leave Recalled Sprint Fidelis ICD Leads in Place? Debate Continues Todd Neale August 28, 2019
News Industry News Medtronic Receives FDA Approval for World's First Quadripolar Active Fixation Left Heart Lead May 01, 2019
News Industry News US Physicians Now Treating Patients with BIOTRONIK's Ultraslim Acticor DX Devices April 29, 2019
News Conference News WRAP IT: Novel Antibacterial ‘Envelope’ Reduces Rate of Infections From Implanted Cardiac Devices L.A. McKeown March 17, 2019
News Daily News Incidental Thrombi on Device Leads Common, but Seemingly Innocuous Todd Neale February 28, 2019
News Daily News Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs Todd Neale February 27, 2018
News Daily News Hurricanes and Wildfires Take Their Toll on Prominent CVD Med-Tech Companies Todd Neale October 19, 2017
News Industry News Medtronic Receives CE Mark for Attain Stability(TM) Quad MRI SureScan(TM) Active-Fixation Heart Lead August 22, 2017
News Daily News FDA Clearance of Modified Devices Relies Heavily on Weak Studies, Surrogate Endpoints Michael O'Riordan August 16, 2017