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The Solia S lead and Selectra 3D catheter have been used in more than 80,000 patients worldwide.
October 9, 2024
By: Michael Barbella
Managing Editor
BIOTRONIK has received U.S. Food and Drug Administration (FDA) labeling approval of its Selectra 3D catheter in conjunction with its Solia S lead for use in left bundle branch area pacing (LBBAP). The two products represent the first and only FDA-approved stylet-driven lead and dedicated delivery catheter system approved for LBBAP, according to the company. “We are committed to physicians with innovative products and solutions, and the Solia S lead with Selectra 3D catheter for LBBAP is a perfect example of physician-driven advancement of care,” BIOTRONIC U.S. President Ryan Walters said. “It is important we meet and support that evolution.” The Solia S lead and Selectra 3D catheter have been used in more than 80,000 patients worldwide.1 The additional indication supports their use in the evolving technique of pacing the heart’s natural conduction system, specifically targeting the left bundle branch area. “Results from the BIO-CONDUCT trial show the Solia S lead and Selectra 3D catheter are extremely reliable and provide excellent outcomes in the setting of LBBAP,” stated Larry Chinitz, M.D., cardiac electrophysiologist and director of NYU Langone’s Heart Rhythm Center in New York City, and BIO-CONDUCT trial lead investigator. “The Solia lead in particular offers several advantages over legacy LBBAP leads, including the ability to continuously pace off the stylet during implantation.” Data from the BIO-CONDUCT study demonstrate a high level of implant success (95.7%) and a low level of lead-related complications (1.7%) of Solia S leads in LBBAP at three months.2 “LBBAP is a therapy on the rise,” BIOTRONIK Chief Medical Officer David Hayes, M.D., concluded. “We are proud to support continuing research into this growing practice and provide the tools for cardiac patients to receive the best possible care.” BIOTRONIK is a global medical technology company with products and services for patients suffering from heart and blood vessel diseases as well as chronic pain. Driven by a purpose to perfectly match technology with the human body, the company develops cardiovascular, endovascular, and neuromodulation solutions. BIOTRONIK is headquartered in Berlin, Germany, and is represented in more than 100 countries. References 1 Data on file. 2 Chinitz L, et al. Left Bundle Branch Area Pacing using a Stylet Driven, Retractable Helix Lead: Results from a Prospective, Multicenter Trial (The BIO-CONDUCT Study). Presented at Heart Rhythm Society; May 19, 2024; Boston, MA.
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