Reverse Medical Corporation Receives FDA IDE Clinical Study Approval For The ReStoreTM Microcatheter

Main Category: Vascular
Also Included In: Regulatory Affairs / Drug Approvals;  Medical Devices / Diagnostics;  Stroke
Article Date: 25 Sep 2009 - 21:00 PDT

email icon email to a friend   printer icon printer friendly   write icon opinions  


Current Article Ratings:

Patient / Public:not yet rated

Healthcare Prof:5 stars

5 (1 votes)


Reverse Medical Corporation announced today that it has received US Food and Drug Administration (FDA) conditional approval to begin a neurothrombectomy IDE study for its ReStore™ Microcatheter at twenty US centers. The study is planned to begin enrollment in US and European hospitals following investigating study center Institutional Review Board (IRB) approvals. Study enrollment will involve approximately 120 subjects which present within eight hours from symptom onset.

Commenting on this significant regulatory milestone, Reverse Medical's Chief Executive Officer Jeffrey Valko said, "This conditional IDE approval of the Reverse Medical ReStore™ Microcatheter represents another important strategic step forward for our rapidly growing Company. We will begin patient enrollment early in 2010, following IRB approvals from our investigating study centers. Reverse Medical will continue to pursue a broadening platform of state-of-the-art endovascular devices for the treatment of neurovascular disorders."

Reverse Medical's scientific and clinical advisor Dr. Satoshi Tateshima, MD, D.M.Sc., Division of Interventional Neuroradiology and UCLA Stroke Center, Ronald Reagan UCLA Medical Center, Los Angeles, CA stated, "In the US, roughly 50% of acute stroke interventions are performed with clot retrievers, and the remainder from a combination of angioplasty, clot aspiration, stenting, and thrombolytic drug delivery. My personal opinion is that the Reverse Medical technology versatility will allow the ReStore™ Microcatheter to cover all of those cases that are currently treated with clot retrievers, suction devices, angioplasty devices and stents."

Reverse Medical has established a strong patent position that surrounds these technology platforms and currently holds one issued and three published US patent applications with an additional nine US patent applications pending publication.

Source
Reverse Medical Corporation

Article adapted by Medical News Today from original press release.
Visit our vascular section for the latest news on this subject.
There are no references listed for this article.
Please use one of the following formats to cite this article in your essay, paper or report:

MLA
Reverse Medical Corporation. "Reverse Medical Corporation Receives FDA IDE Clinical Study Approval For The ReStoreTM Microcatheter." Medical News Today. MediLexicon, Intl., 25 Sep. 2009. Web.
11 Feb. 2012. <http://www.medicalnewstoday.com/releases/165271.php>

APA
Reverse Medical Corporation. (2009, September 25). "Reverse Medical Corporation Receives FDA IDE Clinical Study Approval For The ReStoreTM Microcatheter." Medical News Today. Retrieved from
http://www.medicalnewstoday.com/releases/165271.php.

Please note: If no author information is provided, the source is cited instead.




Vascular

Most Popular Articles



Follow Our Vascular News On Twitter

Follow Us On Twitter
Get the latest news for this category delivered straight to your Twitter account. Simply visit our Vascular Twitter account and select the 'follow' option.



View list of all 'What Is...' articles »