As we blogged at the time, we believe that the Ninth Circuit made a historic error in Stengel v. Medtronic Inc., 704 F.3d 1224 (9th Cir., 2013) (en banc),| Drug & Device Law
Post Market Surveillance (PMS) monitors medical device safety and effectiveness post-market. what's new in 2024?| Sternum IoT
The Pittsburgh Post-Gazette and ProPublica analyzed more than 2 million complaints about medical device malfunctions, patient injuries and deaths submitted to the U.S. Food and Drug Administration’s MAUDE tracking system.| newsinteractive.post-gazette.com
Requirements for reporting medical device problems, including malfunctions and adverse events (serious injuries or deaths) associated with medical devices.| U.S. Food and Drug Administration
These early adopters found out what happened when a cutting-edge marvel became an obsolete gadget... inside their bodies.| IEEE Spectrum
