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SI-BONE, Inc. annuncia il raggiungimento di 10.000 procedure iFuse
Date:1/7/2014

SAN JOSE, California, 7 gennaio 2014 /PRNewswire/ -- SI-BONE, Inc. (San Jose, California), una società di dispositivi medicali pioniera nell'uso di iFuse Implant System®, dispositivo chirurgico a ridotta invasività (MIS) per la fusione dell'articolazione (SI) sacriliaca, ha annunciato oggi che iFuse Implant System è stato utilizzato in oltre 10.000 procedure e sono stati collocati oltre 29.000 impianti iFuse in pazienti in tutto il mondo. La procedura MIS è sempre più adottata a livello globale; oltre 700 chirurghi hanno eseguito la procedura iFuse negli Stati Uniti e in Canada e in 13 paesi europei, e si prevede che altri 4 paesi europei inizino presto a utilizzarla.  La fusione dell'articolazione SI a ridotta invasività è ora considerata la terapia standard[1] per i pazienti che soffrono di sacroileite degenerativa o di rotture dell'articolazione sacroiliaca e che non traggono beneficio dalla terapia conservativa, e l'impianto iFuse, con il suo profilo unico triangolare e il rivestimento con spray poroso al plasma di titanio (TPS), è senza dubbio leader di mercato. In più, iFuse Implant System è l'unico dispositivo utilizzato in fusioni dell'articolazione sacroiliare a ridotta invasività per il quale siano stati pubblicati dati sull'efficacia e sulla sicurezza clinica con revisione da parte di terzi.[2]

"10.000 impianti sono per noi un risultato molto significativo ed è gratificante sapere che i nostri sforzi hanno trattato così tanti pazienti. Tuttavia, nonostante questi importanti successi, riteniamo che vi siano ancora molti pazienti che soffrono di sacroileite degenerativa o di rotture dell'articolazione sacroiliaca che non hanno tratto alcun giovamento dalla terapia conservativa e noi continueremo, in qualità di azienda leader, a informare pazienti, professionisti del settore sanitario e a
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SOURCE SI-BONE, Inc.
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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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