News

May 29, 2007 — The FDA has cleared the CORDIS ENTERPRISE Vascular Reconstruction Device and Delivery System under the Humanitarian Device Exemption — it is used with embolic coils for the treatment of intracranial aneurysms. It consists of a self-expanding stent and a delivery system. The stent serves as a scaffold for embolic coils to prevent herniation of the coils into the parent vessel.

Home May 27, 2007
Home
News

May 29, 2007 — Abbott announced positive results last week from ABSORB, the world’s first clinical trial evaluating the ...

Home May 27, 2007
Home
News

May 23, 2007 — InspireMD has announced this week the enrollment of 19 patients in its First in Man study in a ...

Home May 21, 2007
Home
News

May 22, 2007 — Luna Innovations has announced it has received a market clearance letter in response to its 510(k) ...

Home May 21, 2007
Home
News

May 23, 2007 — MicroMed Cardiovascular Inc. has announced that on Monday, May 14, 2007, doctors at Freeman Hospital in ...

Home May 21, 2007
Home
News

May 23, 2007 — MedicalCV Inc. has announced that the United States Patent and Trademark Office ("USPTO") has issued ...

Home May 21, 2007
Home
News

May 23, 2007 — XTENT Inc. announced positive six-month follow-up data from the CUSTOM II clinical trial, which assessed ...

Home May 21, 2007
Home
News

May 21, 2007 — Sanofi-aventis has announced that the FDA has approved a supplemental New Drug Application (sNDA) for the ...

Home May 20, 2007
Home
News

May 21, 2007 — OrbusNeich announced today it has received CE Mark approval for three interventional cardiology products ...

Home May 20, 2007
Home
News

May 21, 2007 — Findings presented last week during the annual meeting of the Heart Rhythm Society in Denver indicate a common stress test, using GE Healthcare’s latest algorithm for the measurement of T-wave Alternans (TWA), can be useful in predicting sudden cardiac death, even in those without a previous heart attack or symptoms of heart failure.

Home May 20, 2007
Home
News

May 18, 2007 — Inverness Medical Innovations Inc. and Biosite Inc. have announced the companies have entered into a ...

Home May 17, 2007
Home
News

May 18, 2007 — CoreValve has announced that it has received CE Mark approval of its CoreValve Percutaneous ReValving ...

Home May 17, 2007
Home
News

May 18, 2007 — Hansen Medical Inc. said Thursday it obtained approval in the European Union for its Sensei robotic ...

Home May 17, 2007
Home
News

May 18, 2007 — Medicure, a biopharmaceutical company focused on the research, development and commercialization of novel ...

Home May 17, 2007
Home
News

May 18, 2007 — According to a report published Thursday in the Wall Street Journal and posted on UPI, the number of ...

Home May 17, 2007
Home
Subscribe Now