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CVRx(R), Inc. Receives CE Mark Approval for Rheos(R) Baroreflex Hypertension Therapy(TM) System.


MINNEAPOLIS -- CVRx, Inc., a private medical device company, has received CE Mark approval for its Rheos([R]) Baroreflex Hypertension Therapy[TM] System, the only implantable device designed to control hypertension or high blood pressure. The system was approved for marketing in Europe based on clinical studies conducted in Europe and the United States.

"Receiving CE Mark approval is an important milestone for our company," said Nadim Yared, CVRx president and CEO (1) (Chief Executive Officer) The highest individual in command of an organization. Typically the president of the company, the CEO reports to the Chairman of the Board. . "Currently, we are focused on advancing the Rheos Pivotal Trial in the United States. Patient enrollment in the Rheos Pivotal Trial is under way, and we expect outcomes from this study to support our Pre-Market Approval (PMA PMA (papillary-marginal-attached),
n a system of epidemiologic scoring of periodontal disease devised by Schour and Massler in which the symbols denote the areas involved in gingival inflammation.

PMA Progressive muscular atrophy
) application to the FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
."

Recently published abstract results in the Journal of Hypertension showed a significant decrease in blood pressure with the Rheos System at 12 months. One-year results from 13 patients showed a 39 mmHg average decrease in systolic blood pressure Systolic blood pressure
Blood pressure when the heart contracts (beats).

Mentioned in: Hypertension
 and a 26 mmHg average decrease in diastolic blood pressure Diastolic blood pressure
Blood pressure when the heart is resting between beats.

Mentioned in: Hypertension
.1

The Rheos Pivotal Trial and Rheos System

CVRx received investigational device exemption An Investigational Device Exemption (IDE) allows the investigational device to be used in a clinical study in order to collect safety and effectiveness data required to support a Premarket Approval (PMA) application or a Premarket Notification [510(k)] submission to Food and  (IDE) approval from the FDA to begin the Rheos Pivotal Trial that is evaluating the safety and effectiveness of the Rheos System. The trial is enrolling 300 patients at multiple clinical sites in the United States and in Europe. Visit www.rheosstudy.com or call (866) 543-6434 to learn more about the Rheos Pivotal Trial and participant qualifications.

The Rheos System provides a "physiological rational" method to reduce blood pressure. The system's proprietary technology uses the body's own natural blood pressure regulation system (baroreflex) to control blood pressure. The Rheos System includes:

* A small pulse generator Pulse generator

An electronic circuit capable of producing a waveform that rises abruptly, maintains a relatively flat top for an extremely short interval, and then rapidly falls to zero.
 that is implanted under the collar bone;

* Two thin lead wires that are implanted at the left and right carotid arteries and connect to the pulse generator; and

* The Rheos Programmer System, an external device used by doctors to non-invasively regulate the activation energy from the generator to the lead wires.

The system electronically activates the baroreflex, which sends signals to the brain suggesting a blood pressure increase. Then, the brain acts to lower blood pressure by sending signals to various parts of the body to reduce blood pressure, including the blood vessels, heart and kidneys.

Hypertension: The Need for a New Treatment Option

High blood pressure, also referred to as hypertension, affects about 65 million people in the United States alone.2 Hypertension is estimated to cause one in every eight deaths worldwide. Each incremental increase of 20 mmHg in systolic blood pressure or 10 mmHg in diastolic blood pressure above normal levels is associated with a two-fold increase in death rates from stroke, coronary heart disease coronary heart disease: see coronary artery disease.
coronary heart disease
 or ischemic heart disease

Progressive reduction of blood supply to the heart muscle due to narrowing or blocking of a coronary artery (see atherosclerosis).
 and other vascular causes. Approximately 25 percent of people with hypertension cannot control their high blood pressure, despite the use of multiple medications.3, 4

About CVRx, Inc.

CVRx, Inc., is a private company founded in 2001 and headquartered in Minneapolis. Its senior management and technical teams have many years of experience commercializing implantable medical devices. For more information on CVRx visit www.cvrx.com.

Footnotes:

1 Scheffers I, Schmidli J, Kroon kroon  
n. pl. kroon·i
See Table at currency.



[Estonian, from German Krone, from Middle High German kr
 AA, et al. Sustained blood pressure reduction by baroreflex hypertension therapy with a chronically implanted system: Long-term data from the Rheos DEBuT-HT study in patients with resistant hypertension. Journal of Hypertension 2007;25 (Suppl 2):S141-142.

2 Heart Disease and Stroke Statistics. American Heart Association American Heart Association (AHA),
n.pr a national voluntary health agency that has the goal of increasing public and medical awareness of cardiovascular diseases and stroke, and thereby reducing the number of associated deaths and disabilities.
 - 2007 Update.

3 U.S. Renal Data System. USRDS USRDS United States Renal Data System
USRDS US Robotics Dual Standard (modem) 
 2003 Annual Data Report. National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases About NIDDK
The National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), of the U.S. National Institutes of Health, conducts and supports research on many of the most serious diseases affecting public health.
, 2003.

4 Prospective Studies Collaboration. Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies. Lancet 2002;360:1903-1913.

CAUTION: CVRx Rheos System is an investigational device and is limited by Federal (or United States) law to investigational use only.

CVRx, Rheos, Baroreflex Hypertension Therapy are trademarks of CVRx, Inc.

(c) CVRx, Inc. 2007
COPYRIGHT 2007 Business Wire
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2007, Gale Group. All rights reserved.

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Publication:Business Wire
Date:Oct 31, 2007
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