FDA clears Think Surgical robot for use with Medacta knee systems
August 30, 2024
Think Surgical announced that the FDA granted 510(k) clearance for its TMINI miniature robotic system for use with Medacta’s knee systems.
Think Surgical announced that the FDA granted 510(k) clearance for its TMINI miniature robotic system for use with Medacta’s knee systems.
The comprehensive cloud-based platform combines AI diagnostics and detailed measurements for rapid and accurate diagnosis of structural heart disease and heart failure.
Johnson & Johnson MedTech’s DePuy Synthes announced today that it launched its MatrixSternum plate and screw fixation system.
Renata Medical today said the FDA approved its first-of-its-kind Minima growth stent tailored for neonates, infants and young children.
Jupiter Endovascular announced today that the FDA approved an investigational device exemption (IDE) study for its Vertex system.
CereVasc announced today that it received FDA breakthrough device designation for its eShunt system for treating normal pressure hydrocephalus (NPH).
Neuros Medical announced today that it received FDA approval for its Altius direct electrical nerve stimulation system.
A research team at RCSI University of Medicine and Health Sciences has developed a new implant that conveys electrical signals and may have the potential to encourage nerve cell (neuron) repair after spinal cord injury.
INDIANAPOLIS, Aug. 28, 2024 /PRNewswire/ — Prevounce Health, a leading provider of remote care management software, devices, and services, announces the launch of its first blood oxygen device for remote patient monitoring (RPM): Pylo OX1-LTE.
The new ACURATE Prime valve system is indicated to restore function and normal blood flow through a narrowed aortic valve in low, intermediate and high-risk patients with severe aortic stenosis.