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SI-BONE, Inc. annuncia il raggiungimento di 25.000 impianti iFuse
Date:9/10/2013

fetti da disturbi dell'articolazione SI di norma implicano la gestione non chirurgica e, quando i trattamenti non chirurgici dell'articolazione SI non riescono nel loro intento, iFuse può essere un'alternativa all'intervento chirurgico.

iFuse Implant System è un dispositivo disponibile in commercio negli Stati Uniti e in Europa.   La procedura iFuse utilizza una piccola incisione per renderlo disponibile e l'impianto di impianti in titanio. Gli impianti sono rivestiti con uno spray poroso al plasma di titanio che funge da superficie di interferenza, ideata per aiutare a ridurre il movimento dell'impianto e fornire una fissazione immediata e una fusione di lunga durata. Questi impianti hanno un notevole spessore e una metallurgia sofisticata e sono in grado di fornire un costrutto molto più robusto delle viti convenzionali usate per fissare chirurgicamente strutture ossee.  iFuse System serve alla fusione dell'articolazione sacroiliaca per condizioni che comprendono le rotture dell'articolazione sacroiliaca e la sacrilieite degenerativa. Così come con tutte le procedure chirurgiche e gli impianti permanenti, ci sono rischi e considerazioni associati con gli interventi chirurgici e l'utilizzo di iFuse Implant.

Informazioni su SI-BONE, Inc.

SI-BONE, Inc. (San Jose, California) è una società leader per dispostivi medici per l'articolazione sacroiliaca impegnata nello sviluppo di strumenti e prodotti per la diagnosi e la cura dei pazienti con problematiche al dorso inferiore correlate ai disturbi dell'articolazione sacroiliare. La società ha sviluppato e sta producendo e commercializzando approcci meno invasivi che si avvalgono di impianti per il trattamento di alcune patologie dell'articolazione SI. SI-BONE ha un team direzionale esperto con ampia esperienza in di
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2. SI-BONE, Inc. Announces Publication of Postmarket Surveillance Safety Data on First 5,319 Patients Treated with iFuse Implant System
3. SI-BONE, Inc. annuncia la pubblicazione dei dati sulla sicurezza della sorveglianza post-commercializzazione per i primi 5.319 pazienti trattati con il sistema di impianto iFuse Implant System
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