Posted on May 14, 2014 in
Investigations,
Product Liability |
Comments Off on U.S. District Judge Excludes FDA 510(k) Evidence in Medical Device MDL
In an MDL regarding the safety of certain medical devices, the U.S. District Court for the Southern District of West Virginia granted the plaintiffs’ motion in limine to exclude FDA 510(k) evidence related to the FDA’s pre-market notification process on the grounds that the process does not go to the safety or efficacy of medical devices and because of the potential to mislead and...