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

Internet

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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