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Postmarket surveillance of 3D-printed implants for sacroiliac joint fusion

BACKGROUND: Government regulations require postmarket surveillance for cleared/approved medical devices. Trend analysis of newly marketed devices may help to confirm device-related safety or uncover other device or procedure-related problems. METHODS: Complaints related to the use of 3D-printed tria...

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Detalles Bibliográficos
Autores principales:	Cher, Daniel, Wroe, Kendrick, Reckling, W Carlton, Yerby, Scott
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove Medical Press 2018
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168000/ https://www.ncbi.nlm.nih.gov/pubmed/30319290 http://dx.doi.org/10.2147/MDER.S180958

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