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The screw features a new thread design that is more securely fixed into the patient’s vertebral pedicle, reducing the risk of instability caused by bone weakness. Read More
CDRH authorized a record number of novel devices in 2020, issuing 10-fold more Emergency Use Authorizations during the COVID-19 pandemic than in all other previous public health emergencies combined. Read More
Promaxo recently received 510(k) clearance from the FDA for its office-based MRI platform, a device that can be easily set up in office settings without the need for shielding or facility upgrades. Read More
The device is made of stretchable platinum contacts that are encased in a thin film of silicone, enabling high conformability to the surface of the brain. Read More
The French company said that it is launching a multicenter study of Sycamore in France and Germany and expects to be marketing the device globally by 2022. Read More