Medicrea has received 510(k) clearance from the US Food & Drug Administration (FDA) for UNID Hub, a data-driven digital portal for the company’s Adaptive Spine Intelligence (ASI) software.
The UNID Hub is designed to support the surgeon workflow, identify tendencies and correlations and build predictive modelling to drive intelligent strategic decisions and create personalised implant solutions for surgery. The software also serves to enhance the existing proprietary information technology (IT) utilised by the ASI platform for digital surgical planning to create a communication channel between the company’s UNID Lab biomedical engineers and surgeon users to deliver UNID Tek, patient-specific spinal implants manufactured by Medicrea through proprietary rod bending and 3D printing techniques.
The digital communication portal opened with the introduction of UNID Hub is intended to create a sticky, user-friendly environment for surgeons to track and manage their open cases in both snapshot and detailed views, access their complete history with post-operative analyses and dialogue with a dedicated biomedical engineer in real time. UNID Hub has been developed in desktop and mobile applications and should be accessible from medical offices as well as on the go. Future functionalities are planned to become available alongside the software’s wide release planned in October 2017.