Blog Coverage: FDA Approves Boston Scientific's Resonate Family of High-Voltage Devices

Upcoming AWS Coverage on Zimmer Biomet Post-Earnings Results

LONDON, UK / ACCESSWIRE / May 10, 2017 / Active Wall St. blog coverage looks at the headline from Boston Scientific Corp. (NYSE: BSX) as the Company announced on May 10, 2017, that the US Food and Drug Administration (FDA) has given its approval for the Company's Resonate™ line of implantable cardioverter defibrillator (ICD) and cardiac resynchronization therapy defibrillator (CRT-D) systems. Register with us now for your free membership and blog access at:

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One of Boston Scientific's competitors within the Medical Appliances & Equipment space, Zimmer Biomet Holdings, Inc. (NYSE: ZBH), reported on April 27, 2017, its financial results for the quarter ended March 31, 2017. AWS will be initiating a research report on Zimmer Biomet in the coming days.

Today, AWS is promoting its blog coverage on BSX; touching on ZBH. Get all of our free blog coverage and more by clicking on the link below:

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The Approval

Boston Scientific stated that the approval includes new features in the Resonate devices comprising SmartCRT™ technology with Multisite Pacing capability for multi-electrode pacing, and compatibility with the HeartLogic™ Heart Failure Diagnostic Service to support physicians improve heart failure (HF) management. This FDA approval follows on the February 2017 CE Mark and subsequent commercialization for the Resonate family of ICD and CRT-D devices.

In the press release, Boston Scientific noted that every Resonate device is powered by the Company's EnduraLife™ Battery Technology, which has nearly two times the usable battery capacity as certain competitive devices, an essential factor when considering the lifelong needs of patients receiving ICD or CRT therapy. Recent guidance issued by the National Institute for Health and Care Excellence (NICE) in March 2017 recommended the use of EnduraLife-powered CRT-Ds to reduce the number of avoidable replacement procedures a patient may have to undergo, thereby offering improved outcomes for patients and potential savings to the National Health Service (NHS) in England of approximately £6 million in the first five years.

Boston Scientific has also commenced a series of clinical trials, the SMART Registry, SMART CRT Study and SMART MSP, to showcase improved response to CRT therapy with SmartCRT technology. These are expected to help physicians optimize where, when, and how to pace the lower chambers of the heart.

"These trials will add to the body of evidence showing CRT therapy can be tailored to individual patient characteristics at the time of implant, while adjusting device programming solutions over the life of the device without fear of adversely draining the device battery and causing unnecessary replacement procedures," said Dr. Michael Gold, principal investigator of the SMART CRT study and the Michael E. Assey professor of medicine at The Medical University of South Carolina, Charleston.

Furthermore, Kenneth Stein, M.D., Senior Vice President and Chief Medical Officer, Rhythm Management and Global Health Policy, Boston Scientific stated that:

"Our post-approval studies for the HeartLogic service, including MANAGE-HF, will gather additional evidence to illustrate how these alerts, which detect impending heart failure decompensation, can improve patient outcomes."

Stock Performance

At the closing bell, on Tuesday, May 09, 2017, Boston Scientific's stock marginally fell 0.04%, ending the trading session at $26.38. A total volume of 5.43 million shares were traded at the end of the day. In the last six months and previous twelve months, shares of the Company have surged 22.36% and 19.15%, respectively. Moreover, the stock surged 21.96% since the start of the year. At Tuesday's closing price, the stock's net capitalization stands at $36.26 billion.

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