CHICAGO — The use of lumbar drain placement significantly reduces the risk for postoperative cerebrospinal fluid (CSF) leaks in patients undergoing endoscopic endonasal skull base surgery, new ...
BrainSpace, a medtech focused on neurological injuries and illnesses, received 501 (k) clearance from the FDA for its brain ...
BrainSpace announced that the FDA granted 510(k) clearance for its Intellidrop automated brain fluid management system.
BrainSpace, a medical technology company building automated solutions for neuro injury, illness and degeneration, today announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) ...
Please provide your email address to receive an email when new articles are posted on . EARLYDRAIN trial included 287 adults randomly assigned to receive lumbar drainage with standard care or standard ...
Ceribell received breakthrough device designation for its LVO stroke detection monitor, and Naox Technologies secured 510(k) clearance for its in-ear EEG device.
Winner of the Synthes Skull Base Award, Nathan T. Zwagerman, MD, presented his research, A Prospective, Randomized Control Trial for Lumbar Drain Placement after Endoscopic Endonasal Skull Base ...
Charlottesville, VA (August 20, 2013). Researchers at Duke University conducted a randomized clinical trial in patients with subarachnoid hemorrhage (SAH). In this study, the researchers compared two ...