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Spineart is proud to have hosted our first face-to-face event of 2020 in China!

The Cervical Spine Arthroplasty Expert Summit was held in Nanchang on 29^th Nov 2020, involving more than 40 participants. 

During this highly interactive meeting, the participants learned about the history of cervical arthroplasty and were introduced to the latest NMPA (National Medical Products Administration) approved arthroplasty device: BAGUERA® C. 

A combination of presentations on case studies and clinical results, discussion forums on complications, and live surgery gave the participants a deep understanding of the patient benefits, the indications, the surgical steps and pitfalls to avoid when implanting an arthroplasty device. 

The participants enjoyed being able to use the opportunity of the highly professional learning environment to meet together in a more relaxed setting.

En este año único, Spineart se enorgullece de ser patrocinador del congreso GEER una vez más y brindarle la oportunidad de descubrir nuestro stand virtual. Descubra la gama de nuestros productos básicos, nuestros productos más vendidos y nuestras últimas innovaciones. Nos complace compartir que el Dr. Pino presentará los hallazgos del estudio Ti-LIFE en modelo in vivo.

In this unique year, Spineart is proud to sponsor GEER once again giving you the opportunity to discover our virtual booth. Discover our extensive product portfolio including our essentials, our best-sellers and our latest innovations. We’re excited to inform you that the results from our Ti-LIFE animal study will be presented by Dr. Pino.

Following a renewal and two follow–up certification audits recently performed by three independent notify bodies, Spineart is proud to announce that its activities of Design, Manufacturing and Sales of medical implants under ISO 13485 and 93/42/EEC Medical Device Directive have been approved until May 2024.

Spineart is proud to announce the first worldwide surgery using SCARLET® AL-T HL, the new Hyperlordotic Secured Lumbar Anterior Cage.

On November 10^th 2020, surgery with the new SCARLET® AL-T HL Hyperlordotic Secured Lumbar Anterior Cage was successfully performed in the United States by Dr. Jeffrey E Deckey from Orange, CA.

Dr. Deckey commented on the new system that, “The introduction of the Hyperlordotic SCARLET® AL-T cage will provide significant improved options with regards to restoring sagittal balance in spinal deformity.  With varying degrees, one can dial in the correct amount of correction to appropriately match the lumbar lordosis and pelvic incidence.”

SCARLET®AL-T HL is a cage utilizing the Ti-LIFE Technology, an enhanced manufacturing process of titanium cages, based on 3D printing technology, that mimics trabecular bone-like structures.

Following the recent FDA approval to initiate a pivotal IDE clinical study for the BAGUERA® C artificial cervical disc at 1-level, Spineart is proud to announce that it has received approval from the FDA to initiate as well a pivotal IDE clinical study for BAGUERA® C at two contiguous levels.
Both studies will be randomized controlled trials comparing the BAGUERA® C artificial cervical disc to another FDA approved arthroplasty device and they will take place simultaneously at up to 30 centers across the country.

BAGUERA® C Cervical Disc Prosthesis

The BAGUERA® C Cervical Disc Prosthesis is an MRI compatible disc. The endplates of the BAGUERA® C are anatomically shaped and the inner layers 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 adjacent levels

Caution ­Investigational Device, Limited by Federal (or United States) Law to Investigational Use