Reverse Medical said it won CE Mark approval in the European Union for its Barrel vascular reconstruction device.
The Barrel device is designed to be used with occlusive devices when treating intracranial aneurysms, according to a press release.
The Medical Device Business Journal — Medical Device News & Articles | MassDevice
Reverse Medical said it won CE Mark approval in the European Union for its Barrel vascular reconstruction device.
The Barrel device is designed to be used with occlusive devices when treating intracranial aneurysms, according to a press release.
Reverse Medical won European approval for its MVP Micro Vascular Plug system for peripheral artery embolization and the company signed a deal with Century Medical for distribution of its products in Japan.
Penumbra said it won Shonin approval from the Japanese Ministry of Health, Labor and Welfare for its Penumbra Coil 400 intracranial aneurysm device.
The Alameda, Calif.-based medical device company said it plans to launch the device immediately via an exclusive distribution agreement with Japan’s Medico’s Hirata.
The FDA granted 510(k) clearance for Stryker‘s (NYSE:SYK) Trevo Pro blood clot retriever, technology it acquired along with Concentric Medical in 2011.
The medical device company said the stroke treatment device is the latest iteration of its Trevo line, designed to remove the blood clots that cause ischemic stroke.
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