Articles in Headline
Medtronic Infuse Bone Graft Subject to Possible U.S. Senate Investigation
U.S. Senators Charles Grassley, Richard Blumenthal and Herb Kohl have introduced the Medical Device Patient Safety Act, designed to give the Food and Drug Administration (FDA) tools to better monitor post-market performance of new medical …
Medtronic Infuse Bone Graft Caused Uncontrolled Bone Growth, Florida Patient Charges
Jennifer English of Lake Worth, Florida, has filed a complaint against against Medtronic for allegedly misrepresenting the risks and benefits of its Infuse bone graft device and improperly marketing Infuse for non-FDA approved uses.
Study Faults Approval Process for Medical Devices
The government’s system for regulating many medical devices should be abandoned and replaced because it fails to examine their safety and effectiveness before sale, according to one of the nation’s top scientific groups. More…
