Say hello to MassDevice +3, a bite-sized view of the top three med-tech stories of the day. This feature of MassDevice.com’s coverage highlights our 3 biggest and most influential stories from the day’s news to make sure you’re up to date on the headlines that continue to shape the medical device industry.
The U.S. Food & Drug Administration releases a list of 510(k) clearances granted in July 2013.
Japan’s Cyberdyne Inc. lands certification from a German-based medical device certifier, paving the way for the company’s robotic exo-skeleton to march through Europe.
Some lots of Boston Scientific’s Promus Element Plus Monorail stents were shipped with incorrect labeling in Australia, prompting a recall Down Under.