Stryker Receives US FDA HDE Approval ror the Neuroform Atlas(TM) Stent System to Treat Wide Neck Aneurysms

KALAMAZOO, Michigan, USA, Nov. 9, 2017 -- (Healthcare Sales & Marketing Network) -- Stryker Corporation announced today that the U.S. Food and Drug Administration has approved the Neuroform Atlas™ Stent System for marketing under a humanitarian device exe... Devices, Interventional, FDA Stryker, Neuroform Atlas, intracranial aneurysm, embolic coil
Source: HSMN NewsFeed - Category: Pharmaceuticals Source Type: news