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FDA Panel Wants More Data on Mesh Tx for Incontinence, MedPage Today, September 9

MedPage Today (here)  reports an FDA advisory panel meeting over synthetic mesh used to treat stress urinary incontinence (SUI) said it would like more scientific data on the newer generation of devices but recommended leaving in place the 510(k) approval process. FDA Panel Listens to Industry, Patients, Staff The Obstetrics Read more

By | 2011-09-13T01:50:01+00:00 September 13th, 2011|Media Reports|0 Comments