Boston Scientific Announces FDA Approval and First U.S. Implant of New Devices To Treat Bradycardia

NATICK, Mass., May 7, 2012 /PRNewswire/ -- Boston Scientific Corporation (NYSE: BSX) announces U.S. Food and Drug Administration (FDA) approval and market launch of its INGENIO^™ and ADVANTIO^™ pacemakers and INVIVE^™ cardiac resynchronization therapy pacemakers (CRT-P).  The first implant of the INGENIO pacemaker in the U.S. was performed on May 3 by Bruce L. Wilkoff, M.D., Director of Cardiac Pacing and Tachyarrhythmia Devices at the Cleveland Clinic.

To access the multi-media press release, click on the following link: http://www.multivu.com/mnr/43512-boston-scientific-fda-approval-ingenio-advantio-invive-pacemakers.

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Pacemakers are designed to treat bradycardia, a condition in which the heart beats too slowly – usually less than 60 beats per minute – depriving the body of sufficient oxygen.  The INGENIO and ADVANTIO pacemakers feature RightRate™ pacing technology designed to treat chronotropic incompetence (CI).  CI is the inability of the heart to regulate its rate appropriately in response to physical activity, which may cause patients to feel tired or short of breath during daily activities such as walking or climbing stairs.  RightRate employs Boston Scientific's minute ventilation (MV) sensor, the only sensor clinically proven to restore chronotropic competence, and adds programming options to promote ease of use and in-clinic time savings.

"Matching the patient's need to increase their heart rate with their precise activities is the main goal of cardiac pacing," said Dr. Wilkoff, who also serves as the President of the Heart Rhythm Society, and has authored numerous articles on chronotropic response and rate adaptive pacing.  "Achieving that match depends on having the right tools such as an MV sensor and intelligent programming."

In addition to RightRate, the INGENIO pacemaker offers Respiratory Rate Trend (RRT), an exclusive feature that monitors respiration – a key vital sign.  The INVIVE CRT-P offers RRT as part of HF Perspectiv™  – a comprehensive  suite of heart failure diagnostics designed to provide health care professionals with additional information to guide treatment decisions.

"We are very pleased to receive FDA approval for these advanced devices, and excited about the potential they bring to our bradycardia business.  With these products, Boston Scientific embarks on a new era in pacing technology," said Joe Fitzgerald, senior vice president and president of the Boston Scientific Cardiac Rhythm Management group.  "The company's significant investments in the INGENIO platform have been focused on long-term innovation in pacing technologies, and are expected to support a comprehensive series of launches over the next several years to expand our pacing capabilities and help improve patient outcomes."

The INGENIO, ADVANTIO and INVIVE devices are designed for use with Boston Scientific's new LATITUDE™ NXT Remote Patient Management system, which is currently under review by the FDA, and will enable physicians to conduct remote follow-ups of these device patients to monitor specific pacemaker information and heart health status.  The system is designed to detect clinical events between scheduled visits and send relevant data directly to a secure physician-accessible website via landline or cellular-based telephone technology using AT&T's wireless network, under an agreement between Boston Scientific and AT&T. 

In April, the company announced CE Mark approval and European market launch of the INGENIO and ADVANTIO pacemakers and INVIVE CRT-P. 

About Boston Scientific  
Boston Scientific is a worldwide developer, manufacturer and marketer of medical devices whose products are used in a broad range of interventional medical specialties.  For more information, please visit: www.bostonscientific.com.  

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SOURCE Boston Scientific Corporation