Cargando…
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...
| Autores principales: | , , , , , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
SAGE Publications
2022
|
| Materias: | |
| 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 |