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Boston Scientific recalls Vici SDS and Vici RDS venous stent systems following reports of stent migration
According to a medical device recall notice posted on the Food and Drug Administration (FDA) website, Boston Scientific has recalled its Vici venous stent system (Vici SDS) and Vici RDS venous stent system due to reported instances of stent migration.…
Radiation exposure: ControlRad Select imaging system gains FDA market clearance
ControlRad has announced Food and Drug Administration (FDA) 510(k) clearance to market ControlRad Select, a technology that utilizes proprietary semi-transparent filters, a user-interface tablet, and image processing algorithms to reduce radiation exposure during fluoroscopically guided procedures. The technology is retrofitted…