Why 510(k) Loopholes Are Dangerous
Of the two pathways available to medical device manufacturers seeking FDA approval for new products, the 510(k) process is the cheaper and significantly faster route. But, how safe is it?…
Of the two pathways available to medical device manufacturers seeking FDA approval for new products, the 510(k) process is the cheaper and significantly faster route. But, how safe is it?…
With so much whining from the pharmaceutical and medical device industries over the onerous process of Federal Drug Administration (FDA) approval for a new treatment or technology, one would assume…
Kentucky has become the third state to file a civil lawsuit against Johnson & Johnson alleging deceptive marketing of transvaginal surgical mesh used to treat pelvic organ prolapse (POP) and…
This is part two of a multi-part series uncovering common myths related to pelvic mesh. Myth Busters Part One can be found here while Myth Busters Part Three can be…
This is part one of a multi-part series uncovering common myths related to pelvic mesh. Myth Busters Part Two can be found here while Myth Busters Part Three can be…
States file lawsuit against Johnson & Johnson over implants Attorneys General Bob Ferguson of Washington and Kamala Harris of California are the latest officials to take legal action against vaginal…