The SPINEART Navigation Instrument System is a surgical tool used in thoracolumbar spinal surgery to help surgeons accurately locate anatomical structures for the placement of spinal screws. It integrates with the eCential Op.n PERLA® TL Navigation System, which uses intraoperative 3D imaging, to improve surgical precision in both open and minimally invasive procedures.
The SPINEART Navigation reusable instruments are intended to be used during the preparation and placement of SPINEART PERLA TL screws during thoracolumbar spinal surgery to assist the surgeon in precisely locating anatomical structures in either open or minimally invasive procedures. The SPINEART Navigation reusable instruments are specifically designed for use with the eCential Op.n PERLA TL Nav System. It is indicated for population with medical conditions requiring the placement of spinal screws and for which the use of stereotactic surgery may be considered to be appropriate and where reference to a rigid anatomical structure, such as a vertebra, can be identified. The guidance is based on an intra-operative surgical plan developed with Op.n PERLA TL Nav Software and based on intraoperative 3D images provided by a compatible imaging system.
The system consists of reusable surgical instruments used with a navigation system to help locate anatomical structures for spinal screw placement. The new feature is the SPINEART eCential Navigation Adapter, which allows compatibility with the eCential Op.n Navigation System, using intraoperative 3D imaging. The system integrates intra-operative surgical planning and compatible imaging for navigation accuracy.
Performance testing included ASTM F2554 verification of the eCential Navigation Adapter in worst-case scenarios, accuracy verification against acceptance criteria from predicate devices, and no clinical testing was required. Testing confirmed navigation accuracy with the eCential Op.n Perla TL Nav System is equivalent to the predicate Medtronic StealthStation System.
No predicate devices specified
Submission
9/23/2024
FDA Approval
3/7/2025
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