The DIVA device, class IIb medical device, is a system of cages which are intended to be implanted in the spine via various approaches (PLIF, ALIF, TLIF, XLIF, Corpectomy Lumbar, Corpectomy Cervical, and ACIF) in order to help achieve vertebral fusion between two or more vertebras. Spinal fusion aims to
reduce significantly and sustainably patient’s pain and disability.

This surgery, performed by orthopedic surgeons or neurosurgeons on skeletally mature patients, could be conducted in the thoracolumbar or the cervical region of the spine. Specific implants have been designed, developed and distributed by Novaspine for each of these treated areas and according to
the surgical approach. Medical indications, contraindications, general adverse events, lifetime and safety measures are gathered in the IFU provided with the DIVA system. Performance claims focuses on fusion rate, pain reduction and disability reduction, while safety claims concern cage breakage,
subsidence or migration rates.

All the DIVA products have been CE marked and implanted since 2006.