NuVasive’s Surgical Automation Platform Cleared by FDA

July 27, 2018

The FDA granted 510(k) clearance for Pulse, NuVasive’s surgical automation platform, which combines 2D and 3D navigation and smart imaging capabilities.

Used for spinal surgery, the device includes multiple technologies with features that allow wifi and independent device access.

Pulse addresses visualization problems during surgery by using multiple high-resolution cameras to allow surgeons an uninterrupted line of sight.

View today's stories