Device for treating challenging bone fractures cleared by FDA
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The Bone Bolt System received an FDA 510(k) clearance to sell and market the device, marking it the first for a brand new medical device in the U’s history.
Read MoreThe Bone Bolt System received an FDA 510(k) clearance to sell and market the device, marking it the first for a brand new medical device in the U’s history.
Read MorePOWDERED GLOVE BAN As of Jan. 18, 2017, the Food and Drug Administration (FDA) has banned the use of powdered patient examination gloves, as well as absorbable powder for lubricating gloves. The FDA determined that the powder presented an unreasonable and substantial risk of illness or injury that cannot be corrected or eliminated by labeling or […]
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