Posts Tagged ‘ Transvaginally ’

FDA Approves New American Medical System Transvaginal Mesh Sling

Dec 9th, 2013 | By
FDA Approves New American Medical System Transvaginal Mesh Sling

American Medical Systems (AMS) has just received FDA clearance to market a new incontinence sling, according to a press release that appears in the Wall Street Journal. The RetroArc Retropubic Sling System received the Food the Drug Administration’s 510(k) clearance, a standard that does not require any clinical trials but relies on naming a similar 
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Op-Ed: Dr. Shezad Malik on Doctors and Transvaginal Mesh

Jul 2nd, 2013 | By
Op-Ed: Dr. Shezad Malik on Doctors and Transvaginal Mesh

Op-Ed: Dr Shezad Malik Law Firm http://www.shezadmalik.com/ Dr. Malik is a cardiologist and now an attorney in Dallas who heads his own law firm. He is board certified in internal medicine and was a practicing cardiologist for 10 years. In 2003 he decided to go to law school and has been practicing personal injury law
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Mesh Medical Device News Desk: What’s New

Sep 18th, 2012 | By
Mesh Medical Device News Desk: What’s New

Welcome to Mesh Medical Device News Desk We’ve been a little more than a year since we first established this website and from the traffic, comments and phone calls it appears the number of mesh-injured folks keeps rising. There isn’t a day that goes by when I don’t hear from someone who is desperate for
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Public Citizen: Recall Synthetic Surgical Mesh

Aug 25th, 2011 | By
Public Citizen: Recall Synthetic Surgical Mesh

AUGUST 25, 2011 – Synthetic surgical mesh is implanted into women for the treatment of pelvic organ prolapse and incontinence and now Public Citizen is calling for a ban citing the needless exposure of patients to serious, life-altering complications. Synthetic mesh used for pelvic surgeries, and hernia repair in men, is made of a petroleum-based
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We hope you find this a helpful resource. National News Editor, Jane Akre, began MDND with the hope of providing the latest news, information and perspective from the regulatory, industry and patient point of view, something that goes under-reported in much of the coverage of medical devices. The public is just now becoming aware that many devices do not undergo the same scrutiny as prescription drugs and are instead grandfathered in under an FDA loophole that has gone largely unchanged since the 1970s. As a result, patients become the post-market clinical trial subjects, and many suffer devastating and permanent injuries.