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SI-BONE, Inc. franchit le cap des 10 000 interventions chirurgicales
Date:1/6/2014

tefois, malgré cette réussite considérable, nous savons qu'il existe encore un grand nombre de patients atteints de dégénérescence sacro-iliite ou de dislocations de l'articulation sacro-iliaque pour lesquels la thérapie traditionnelle a échoué, et nous continuerons nos efforts de sensibilisation auprès des patients, des professionnels de santé et des assureurs quant aux avantages d'iFuse en tant qu'option de traitement en faveur de ces patients, » a déclaré Jeffrey Dunn, président et PDG de SI-BONE.

Steven Garfin, docteur en médecine, professeur émérite et président du Département de chirurgie orthopédique de l'UC de San Diego, a déclaré : « Il y a un peu plus de quatre ans, j'ai été intrigué lorsque j'ai découvert pour la première fois SI-BONE et la procédure iFuse, et j'ai pensé qu'il s'agissait d'une avancée utile destinée seulement à un nombre très limité de patients. Pourtant aujourd'hui, un peu plus de quatre ans après et à l'issue de plus de 10 000 interventions, il est clair que les troubles de l'articulation SI qu'il est possible de traiter avec iFuse sont bien plus répandus que ce que nous le pensions autrefois. La société SI-BONE est à l'origine de cette nouvelle approche en faveur du traitement de l'articulation SI, et l'iFuse constitue l'unique dispositif CMI ayant publié des preuves cliniques appuyant sa sécurité et son efficacité d'utilisation. Je suis impressionné par les efforts fournis par la Société en faveur des patients. »

SI-BONE, Inc. a initialement obtenu une approbation 510(k) en novembre 2008 de la part de la Food and Drug Administration (FDA) pour la commercialisation de s
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