The Complex Process of Using the Interconnected Knee Arthroplasty Device Clearance Pathway

Background: The clearance of medical devices by the US Food and Drug Administration (FDA) has remained largely unchanged since 1976, when the Medical Device Amendments Act established a system classifying devices into 3 categories based on safety risk to the consumer. The system allows for the clear...

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Detalles Bibliográficos
Autores principales: Zhu, Andrew, Ying, Xiaohan, Pean, Christian A., Sheth, Neil P., Cross, Michael B., Gonzalez Della Valle, Alejandro, Premkumar, Ajay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527547/
https://www.ncbi.nlm.nih.gov/pubmed/36258781
http://dx.doi.org/10.1177/15563316221099014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9527547/
https://www.ncbi.nlm.nih.gov/pubmed/36258781
http://dx.doi.org/10.1177/15563316221099014

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