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 Spineart has successfully completed over 1,000 TRYPTIK®2 C-PLATE surgeries in the US. 

TRYPTIK®2 C-PLATE is the first cervical plating system offered by Spineart in the US. The system features low-profile plates and one-step, integrated locking rings to prevent screw back out. With streamlined instrumentation and sterile-packed implants, TRYPTIK®2 C-PLATE offers surgeons and operating room staff a practical solution for anterior cervical pathologies.

More information on TRYPTIK®2 C-PLATE on : https://www.spineart.com/us/products/tryptik2-ac-p/

Spineart is excited to host our next Spineart Online Training Webinar on Friday 26th February.

Join us for this interactive session (in English) on the topic of BAGUERA® C as our speakers discuss the latest clinical results and their surgical experiences, giving you the chance to ask questions about what you can expect to achieve for your patients.

Spineart is proud to announce the first cervical disc arthroplasty surgery performed at the Smooha University Hospital, Alexandria Egypt using the BAGUERA® C cervical disc prosthesis.

Dr Samer Samy successfully performed the procedure and commented, “I liked the simplicity and ease of application of the BAGUERA® C which made the procedure safe and effective.” 

The BAGUERA® C Cervical Disc Prosthesis is an MRI compatible spinal device. The endplates of the BAGUERA® C are anatomically shaped and their inner bearing surfaces are coated with a diamond-like material that features a low coefficient of friction. The load sharing design and the guided mobile nucleus are intended to prevent excessive constraints on the facet joints and the adjacent levels. 

Discover more information on BAGUERA® C

After getting the CE marking, Spineart is proud to announce that we received the FDA 510(k) clearance for the new Minimal Invasive Thoracolumbar Posterior Fixation System, PERLA® TL MIS on January 15^th, 2021.

PERLA® TL MIS is a comprehensive system including polyaxial screws with Extended Tabs which enable a connection to different rod diameters. It contributes to the treatment of spinal pathologies through Percutaneous and Minimal Invasive Surgeries and perfectly complements the new PERLA® TL solutions designed for the treatment of degenerative pathologies.

Further extensions of the PERLA® TL solution are expected to come.

After getting the CE marking, Spineart is proud to announce that we received the FDA 510(k) clearance for the new Minimal Invasive Thoracolumbar Posterior Fixation System, PERLA® TL MIS on January 15^th, 2021.

PERLA® TL MIS is a comprehensive system including polyaxial screws with Extended Tabs which enable a connection to different rod diameters. It contributes to the treatment of spinal pathologies through Percutaneous and Minimal Invasive Surgeries and perfectly complements the new PERLA® TL solutions designed for the treatment of degenerative pathologies.

Further extensions of the PERLA® TL solution are expected to come.

On January 11th 2021, Dr Juan M Valdivia Valdivia MD., FAANS. neurosurgeon, successfully performed the first worldwide procedure with PERLA® in Tampa, FL, United States of America. 

The PERLA® system allows to fuse from occiput to thoracic spine. After the procedure, a fusion from Occiput to C4, Dr. Valdivia noted that, «the Perla Occipital Plate is a user friendly system. The angle instrumentation was particularly useful to the success of the procedure”. 

The PERLA® posterior occipito-cervico-thoracic fixation system is intended to provide immobilization and stabilization of spinal segments as an adjunct to fusion for the following acute and chronic instabilities of the cranio-cervical junction, the cervical spine (C1 to C7) and the thoracic spine (T1 to T3).