Life Sciences

FDA issues public health watch for transvaginal placement of surgical mesh

Device Regulation Alert: Safety, Compliance and Reimbursement News, October 27, 2008

Nine surgical mesh manufacturers submitted more than 1,000 reports of complications associated with surgical mesh devices used to repair pelvic organ orolapse and stress urinary incontinence in the last three years, according to an FDA public health notification.

Post a Comment

Name:

 

E-mail:

 

Please enter your comment below:

   

Please enter the text below:

   
   

Most Popular