The objective of the current study was to develop an in vitro testing
protocol to evaluate semi-rigid pedicle screw devices. A corpectomy mo
del protocol exists to evaluate rigid spinal implants: however, semi-r
igid devices are contraindicated for this condition. This paper descri
bes a technique that simulates more closely the conditions a semi-rigi
d device would see in vivo. Finally, the new testing protocol is used
to evaluate the DDS(R) pedicle screw-cable system. Benefits and shortc
omings of the new protocol are discussed.