Robert M. Starke, M.D., M.Sc., an experienced neurosurgeon and researcher with the University of Miami Health System and Miller School of Medicine, has been conducting laboratory studies on a ...

Medtronic recalled a brain aneurysm stent device Sept. 20 because of a risk of malfunction that has been linked to 10 serious injuries and two deaths. The company recalled its Pipeline Flex ...

November 2, 2011 — A new stent graft system approved by the US Food and Drug Administration (FDA) yesterday solves a human plumbing problem that makes it harder to treat patients with an abdominal ...

The FDA approved Stryker’s stent system that, along with neurovascular embolic coils, treats multiple types of aneurysm. The nod comes under a humanitarian device exemption (HDE). The Neuroform Atlas ...

The use of flow-diverting stents to treat intracranial aneurysms appears safe and highly successful. Ischemic complications occur in brain territories supplied by the parent artery in which the stent ...

The US Food and Drug Administration (FDA) has issued a series of recommendations for use of neurovascular stents for stent-assisted coiling (SAC) of unruptured aneurysms after the agency received ...

An increasing number of patients with thoracic aortic aneurysms are being treated with a device called a stent graft, rather than open-chest surgery. The device is delivered with a cathether. Patients ...

After Susan Wakulich was told she had an aneurysm, she figured an invasive brain surgery and lengthy recovery lay ahead of her. "I was devastated," said Wakulich, who is 56 years old and lives in ...

According to MarketsandMarkets™, the peripheral vascular devices market is projected to grow from about USD 10.02 billion in 2026 to USD 13.22 billion by 2031, at a CAGR of 5.7%.

Robert M. Starke, M.D., M.Sc., an experienced neurosurgeon and researcher with the University of Miami Health System and Miller School of Medicine, has been conducting laboratory studies on a ...