CraniUS Therapeutics Receives FDA 510(k) Clearance for the CraniUS® Plate, a Patient-Specific Cranial Implant
News from PR Newswire FDA: CraniUS Therapeutics Receives FDA 510(k) Clearance for the CraniUS® Plate, a Patient-Specific Cranial Implant
Neurotechnology company based in Baltimore developing NeuroPASS platform for direct-to-brain therapeutic delivery, bypassing the blood-brain barrier to treat neurological diseases. First fully implantable platform for long-term, programmable drug delivery. Closed $20M Series B.
News from PR Newswire FDA: CraniUS Therapeutics Receives FDA 510(k) Clearance for the CraniUS® Plate, a Patient-Specific Cranial Implant