The FDAnews report EU MDR Compliance can help. Our editors have combed through the regulations, picking out the most minute compliance points and building them into a checklist of 200+ requirements you can use to confirm that you are satisfying all the EU mandates for device manufacturing.
Stryker Neurovascular announced that its Trevo Pro Retriever has been granted 510(k) market clearance by the FDA. The Trevo Pro Retriever is the next generation in clot removal technology from Stryker. The Sacramento Bee