VEOS TITANIUM is a top loading posterior osteosynthesis system that can be used in open or percutaneous/minimal invasive surgery. VEOS is part of the VEOS-KAPHORN modular platform of implants and instruments, offering a versatile solution to adapt to surgeon’s needs: several specific implants and instruments modules are organized around a universal base.
Fully modular, the platform aims to offer a wide range of possibilities in terms of technologies, surgical approaches and treatment solutions.
Implants material
• Titanium alloy TA6V (ISO 5832-3 et ASTM F136).
Instruments material
• Stainless steel (EN 10088-2, EN 10216-5, ASTM A213), titanium (5832-3 or 5832-2), polymers
Indications
VEOS system can be used in skeletally mature individuals (adults) and in adolescent population for specific indications such as scoliosis.
This medical device is intended for the posterior fixation of the thoracic, lumbar and sacral spine. It is indicated for the treatment of
• Deformities (any etiology)
• Trauma
• Tumors
• The degenerative spine (spondylolisthesis, degenerative disc disease, spinal fractures, spinal stenosis, non-union).
• VEOS can also be used in revision surgery in case of failure of a previous procedure.
Features
- 2 screw options: solid and cannulated-fenestrated
- Polyaxial, monoaxial and polyaxial reduction screws
- Double threaded solid screw
- Quadruple and double threaded cannulated screw
- A complete range of rod-to-rod connectors: axial, parallel and transverse
- Versatile sacro-iliac fixation: different options of iliac and sacral fixation, 2 or 3-points of sacro-iliac fixation
Product Range
- 5 screw diameters (ø4.5 to 8.5 mm) of polyaxial, monoaxial et polyaxial reduction screws
- Titanium alloy rods (ø5.5 mm) :
- Straight (L 40-500 mm)
- Pre-bent (L40-130 mm)
- Ultra-bent at 60° and 90° (L 150-200-250 mm)
- Rod-to-rod connectors: axial, parallel and transverse
- Versatile sacro-iliac fixation system: iliac fixation with VEOS tulip screw or sacral screw, polyaxial and monoaxial sacral plates, modular sacro plate, sacral screws
About Spineway Group
About Spineway :
Spineway is an independent French company, founded in Lyon in 2005, and dedicated to the design and development of advanced technologies for spine surgery. Backed by 100% French know-how, we have contributed to more than 125,000 surgeries over the past 20 years. With the acquisitions of Distimp in 2021 and Spine Innovations in 2022, we have broadened our offering by combining complementary product portfolios and territories, while offering solutions to treat new pathologies.
Our CE0459 certified medical devices reflect our commitment to quality and safety. Spineway also holds 14 patent families in France and abroad, testifying to our commitment to innovation.
Spineway positions itself as much more than just a manufacturer, establishing close partnerships with surgeons. We offer an international program of customized training courses in surgical techniques, to meet the exact requirements and expectations of practitioner. Our 40 enthusiastic employees work side by side with you, listening to your expectations, to co-construct solutions adapted to a constantly evolving practice.
As a company on a human scale, we value the development of our teams, enabling them to give the best of themselves. Together, we are committed to improving the quality of care and advancing medicine.
About Spine Innovations
Spine Innovations is the manufacturer of the ESP disc protheses.
The ESP disc prothesis is the result of 10 years of collaborative research work at the Hôpital Pitié Salpêtrière in Paris, the French Atomic Energy Commission (CEA) and the Université Paris VI, and was driven by the Oséo Innovation contest in France.
Unlike traditional articulated prostheses composed of moving metal parts, ESP prostheses use a viscoelastic core designed to replicate the biomechanical behavior of a healthy intervertebral disc.
This technology is specifically designed to:
- preserve mobility in the operated segment;
- replicate the six physiological degrees of freedom;
- provide shock absorption similar to that of a natural disc.
The LP-ESP (lumbar prosthesis) received its CE marking in 2007 and the CP-ESP® (cervical prosthesis) in 2012.
In 2020, Spine Innovation, an independent company, was founded to focus on the development, production, and marketing of ESP prostheses.
In July 2022, Spineway acquired 100% of Spine Innovations as part of its external growth strategy.
About Distimp
From its inception in 2018, Distimp has focused on offering innovative solutions while drawing on a strong network of surgeons, particularly in France and Europe.
Spineway finalized the acquisition of 100% of Distimp in June 2021.
This transaction served several strategic objectives:
- to expand the group’s product portfolio;
- to strengthen its presence in the French market;
- to benefit from the network of surgeons developed by Distimp;
- to enhance its offering with new technical solutions for spinal surgery.