Brainlab recalled Spine & Trauma 3D Navigation 1.0 software due to the potential for incorrect information to display during surgery, preventing acccurate navigation of surgical tools inside the patient. FDA has identified this as a Class I recall.
SI-BONE received an additional FDA 510(k) clearance for use of iFuse Bedrock technology in fusion of the sacroiliac joint during long construct procedures.
EOS imaging launched EOSlink to integrate EOSapps pre-op surgical planning software with tools like navigation and robotics-based systems for spine, total hip and total knee procedures.