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Boston Scientific Announces FDA Approval of New Heart Failure Lead
Boston Scientific Announces FDA Approval of New Heart Failure Lead
NATICK, Mass., May 16 /PRNewswire-FirstCall/ -- Boston Scientific
Corporation (NYSE: BSX) today announced U.S. Food and Drug Administration
(FDA) approval of its ACUITY(R) Spiral left ventricular lead for use with
cardiac resynchronization therapy defibrillators (CRT-D) and cardiac
resynchronization therapy pacemakers (CRT-P), both of which treat heart
failure. The ACUITY Spiral lead is the Company's fifth generation left
ventricular lead and second in the ACUITY family of left ventricular leads.
The product features a spiral fixation design and small lead tip profile (4.1
French tapering to 2.6 French) for placement of the lead in veins of varying
sizes, including difficult-to-access veins. A lead is an insulated wire that
carries the heart signal to the implanted device and delivers energy from the
device to the heart. In most cases, leads are passed into the heart through
veins.
"In the U.S. clinical trial, the ACUITY Spiral fixation design provided
excellent stability after implant," said John Hummel, M.D., principal
investigator of the ACUITY Spiral U.S. clinical trial. "ACUITY Spiral has the
smallest left ventricular lead tip profile in the industry, offering greater
flexibility to place the lead in veins I may have avoided in the past."
Boston Scientific is also conducting a prospective, multi-center trial
designed to collect and analyze real-world performance data for the ACUITY
Spiral lead. The study will enroll approximately 1,700 patients in up to 125
centers. Patients will be followed over a period of five years and will be
enrolled on Boston Scientific's LATITUDE(R) Patient Management system,
enabling wireless remote management of patients.
"This study demonstrates Boston Scientific's commitment to quality and
robust post-market surveillance of new leads," said Arjun Sharma, M.D., Vice
President, Patient Safety, Boston Scientific CRM. "The data from this post-
market study will provide us with a deeper understanding of the lead's
performance in real-world practice and will be a welcome addition to the data
we collected from the U.S. clinical trial."
Boston Scientific is the only company to offer four fixation designs that
provide stability in a variety of venous anatomies, enabling physicians to
select the most appropriate lead for their patients. The ACUITY Spiral lead
is designed for use with heart failure devices, such as the COGNIS(TM) CRT-D,
which received FDA approval earlier this week.
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.
Cautionary Statement Regarding Forward Looking Statements
This press release contains forward-looking statements within the meaning
of Section 21E of the Securities Exchange Act of 1934. Forward-looking
statements may be identified by words like "anticipate," "expect," "project,"
"believe," "plan," "estimate," "intend" and similar words. These
forward-looking statements are based on our beliefs, assumptions and estimates
using information available to us at the time and are not intended to be
guarantees of future events or performance. These forward-looking statements
include, among other things, statements regarding our product performance,
regulatory approval of our products, new product launches, competitive
offerings, our growth strategy, and our market position. If our underlying
assumptions turn out to be incorrect, or if certain risks or uncertainties
materialize, actual results could vary materially from the expectations and
projections expressed or implied by our forward-looking statements. These
factors, in some cases, have affected and in the future (together with other
factors) could affect our ability to implement our business strategy and may
cause actual results to differ materially from those contemplated by the
statements expressed in this press release. As a result, readers are
cautioned not to place undue reliance on any of our forward-looking
statements.
Factors that may cause such differences include, among other things:
future economic, competitive, reimbursement and regulatory conditions; new
product introductions; demographic trends; intellectual property; litigation;
financial market conditions; and, future business decisions made by us and our
competitors. All of these factors are difficult or impossible to predict
accurately and many of them are beyond our control. For a further list and
description of these and other important risks and uncertainties that may
affect our future operations, see Part I, Item 1A - Risk Factors in our most
recent Annual Report on Form 10-K filed with the Securities and Exchange
Commission, which we may update in Part II, Item 1A - Risk Factors in
Quarterly Reports on Form 10-Q we have filed or will file thereafter. We
disclaim any intention or obligation to publicly update or revise any
forward-looking statements to reflect any change in our expectations or in
events, conditions, or circumstances on which those expectations may be based,
or that may affect the likelihood that actual results will differ from those
contained in the forward-looking statements. This cautionary statement is
applicable to all forward-looking statements contained in this document.
CONTACT: Paul Donovan
508-650-8541 (office)
508-667-5165 (mobile)
Media Relations
Boston Scientific Corporation
Larry Neumann
508-650-8696 (office)
Investor Relations
Boston Scientific Corporation
SOURCE Boston Scientific Corporation
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