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BioWorld - Thursday, December 25, 2025
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Home » FDA greenlights Balt’s STEM trial for subdural hematoma
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FDA greenlights Balt’s STEM trial for subdural hematoma

May 18, 2020
By Meg Bryant
Balt USA LLC, of Irvine, Calif., has received a thumbs up from the FDA to begin an IDE trial of its Squid liquid embolic device for the treatment of chronic subdural hematoma (cSDH). The nonadhesive agent offers a minimally invasive option for a disabling neurological condition that often requires brain surgery to correct.
BioWorld MedTech Clinical Regulatory Neurology/psychiatric FDA IDE

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