News

Spineart is delighted to confirm the outstanding success of its latest Spineart Academy course held in Madrid on April 9th-10th 2015.

This meeting brought together 41 participants from 13 different countries and was mainly focused on Deformities, Minimally Invasive Surgery and Cervical spine. As a result, 32 surgeons were trained on ROMEO®2 and JULIET® portfolios as well as on our latest product launched SCARLET® AC-T, a full titanium secured cervical cage.

Moreover, the 2 years follow up clinical and radiological results on our BAGUERA®C disc prosthesis has been introduced to the audience.

Spineart announced the completion of the regulatory approval process in India for its ROMEO®2 thoraco-lumbar system and its unique ROMEO®2 MIS K-Wireless technology, its full range of JULIET® lumbar cages, its full cervical fusion range TRYPTIK® and its flagship artificial cervical disc BAGUERA®C.

Spineart is now poised to address successfully this promising market in partnership with its local distributor.

Last week Spineart hosted a lab in Austin where 23 participants from Mexico and New Zealand had the opportunity to learn more about the latest innovations in total cervical disc replacement and anterior cervical discectomy fusion, management of adult scoliosis and minimally invasive treatment methods for degenerative conditions as well as benefits of sterile packaged barcoded implants.

All participants had the opportunity to train on M.I.S. surgical techniques through interactive presentations and hands-on anatomical workshops. Thanks to prominent surgeon faculty from the USA and France the course proved very informative for each participant.

In November Spineart hosted a lab in San Diego where 52 participants from the USA, Brazil, Mexico, Colombia, Chile, Slovakia and Malaysia had the opportunity to learn more about the latest innovations in total cervical disc replacement and anterior cervical discectomy fusion, management of adult scoliosis and minimally invasive treatment methods for degenerative conditions as well as benefits of sterile packaged barcoded implants.

All participants had the opportunity to train on M.I.S. surgical techniques through interactive presentations and hands-on anatomical workshops with the support of prominent surgeon faculty from the USA, Mexico, France & Germany. This was the largest international course hosted by Spineart to date.

Spineart is pleased to announce the world’s first implantation of the titanium version of the ROMEO®2 PAD, at the Lawrence + Memorial Hospital in New London, CT (USA).

ROMEO®2 PAD Ti is a Titanium posterior non pedicle supplemental fixation device intended for use as an adjunct to fusion in the lumbar spine.

Patrick F. Doherty, MD, neurosurgeon, successfully performed the procedure. After the surgery, Dr Doherty commented: “I have performed over 150 interspinous fusions since 2010. This device excels at allowing better placement against the spinous process due to the polyaxial nature of the implant, and provides better purchase into the spinous process due to the teeth pattern and height. ROMEO®2 PAD Ti provides an excellent alternative to pedicle screws via a midline, minimally invasive approach.”

All Spineart implants are sterile packed and bar-coded for increased safety, procedure compliance and cost effectiveness.

For more information, please contact us at contact@spineart.com or visit spineart.com.

Spineart is pleased to announce the FDA approval of the SCARLET® AC-T cervical secured cage system. The SCARLET®AC-T combines the benefits of an interbody device and cervical plate in one implant. The locking mechanism of the screw head is completely integrated within the cage, reducing the profile and potential risks associated with dysphagia. The Titanium sandblasted surfaces of the implant facilitate primary stability and osseointegration.

The instrument set is designed according to Spineart’s philosophy of simplicity, featuring one compact box of intuitive instruments.