Citing evidence that patients may have an adverse biological response to certain types of metals, FDA announced that it is taking a closer look at materials used in medical devices, specifically metal-on-metal and nitinol.
A recap of three spine and three trauma products of interest that have gained FDA clearance since January. Devices include a spine cage from a traditionally biologics company, a foot/ankle device from a spine company, and additively-manufactured and computer assisted surgery products.
Technology and talent could impact supply chain management departments in 2019. An industry veteran shares what you need to know to ensure that products are manufactured, packaged and delivered to your customers to spec and on time.