Medtronic, Contego claim new FDA nods for Neuroguard carotid stent

Contego Medical has secured new green lights from the FDA for its Neuroguard IEP stent and filter system, broadening its use in treating narrowed carotid arteries.

Exclusively sold by Medtronic (NYSE: MDT), the device’s implant, delivery and blood flow reversal system picked up a premarket approval, while its umbrella-like filter designed to stop clots and other particles from reaching the brain obtained an additional 510(k) clearance.

Contego’s three-in-one approach combines a nitinol stent, balloon and a 40-micron embolic filter, which together aim to protect the brain during a transcarotid artery revascularization procedure, or TCAR, by temporarily redirecting the flow of blood away from the head and catching floating debris.

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