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Infuse for TLIF initially received FDA breakthrough device designation in April 2024. A new indication could expand treatment ...
Clearance by the Food and Drug Administration means a Stewartville manufacturer can now sell its fecal incontinence devices in the US, after years of being limited to the European market. "It is a ...
The Y-90 resin microspheres demonstrated a 98.5% best overall objective response rate, with all patients responding to the treatment.
From softwares to implants, here are 10 spine products earning FDA nods since May 15. 1. Accelus’ FlareHawk interbody fusion device was FDA-cleared for use in MRI scanning under certain conditions.
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Futurism on MSNThe FDA Is Using an AI to "Speed Up" Drug Approvals and Insiders Say It's Making Horrible MistakesInsiders at the Food and Drug Administration are ringing alarm bells over the agency's use of an AI to fast-track drug ...
From softwares to implants, here are 10 spine products earning FDA nods since May 15. 1. Accelus’ FlareHawk interbody fusion device was FDA-cleared for use in MRI scanning under certain conditions.
The Trump administration‘s “Make America Healthy Again” goals depend on negotiations with food and healthcare industry leaders rather than regulation, the heads of the Food and Drug Administration and ...
Health officials say smoking has been at a high rate in Eastern Kentucky and e-cigarettes are still considered dangerous.
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