Stryker Neurovascular

Stryker Neurovascular — FDA 510(k) Submissions

Stryker Neurovascular has submitted 32 FDA 510(k) premarket notifications since 2011, of which 32 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Device, Neurovascular Embolization, Catheter, Percutaneous, Neurovasculature, Catheter, Percutaneous, Neurovascular Mechanical Thrombectomy Device For Acute Ischemic Stroke Treatment, Catheter, Thrombus Retriever . Use the specialty filter in the sidebar to narrow results.