References 584% CONFIDENCEOverall confidence: 84%How well the pin's source and references back up its dates.Weighted average of how firmly 5 references, the source included, support the pin's start and end times; a reference counts half as much for every 180 days older than the newestShow all pins at 75% confidence or better

The first entry is always the pin's source. Overall confidence is a weighted average of how firmly each reference supports the start and end times used above; a reference counts half as much for every 180 days older than the newest.

• [1]90%
  abbott.mediaroom.com/2025-12-22-Abbotts-Volt-TM-Pulsed-Field-Ablation-System-Receives-FDA-Approval-to-Treat-Patients-with-Atrial-Fibrillation

  abbott.mediaroom.com· Posted Sep 23, 2026· Starts Dec 22, 2025 ✓· 33% of score

  The release is datelined "ABBOTT PARK, Ill., Dec. 22, 2025" and says Abbott "today announced" the FDA^[5] has approved the Volt PFA System (the FDA's own record gives a decision date of 12/19/2025).

• [2]75%
  First Canadian Commercial Use of Abbott's Volt Pulsed Field Ablation System Advances Minimally Invasive Atrial Fibrillation Care

  abbott.mediaroom.com· Published Sep 15, 2026· 32% of score

  Abbott's later release on Volt's first Canadian use at the McGill University Health Centre, noting Health Canada authorization in April 2026 and availability in the U.S., Europe and Australia.^[1]

• [3]82%
  Volt Pulsed-Field Ablation System Gains FDA Approval

  tctmd.com· Published Dec 24, 2025· 12% of score

  TCTMD's report of the approval with the VOLT-AF IDE 6-month effectiveness and safety results behind it.

• [4]85%
  Abbott receives FDA approval for Volt PFA system

  medtechdive.com· Published Dec 22, 2025· 12% of score

  MedTech Dive's report of the approval, placing it against Medtronic, Boston Scientific and J&J in the U.S. PFA market.

• [5]95%
  Premarket Approval (PMA) P250022: Volt PFA System

  accessdata.fda.gov· Published Dec 19, 2025· 11% of score

  The FDA's PMA database entry for the Volt PFA System: applicant Abbott Medical, decision date 12/19/2025, and the approved indication.

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