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Recall Rates of Total Knee Arthroplasty Devices Are Dependent on the FDA Approval Process
Introduction The medical device industry has grown substantially in recent years. There is limited research examining orthopedic subspecialties and the recall of orthopedic devices. We hypothesize that knee arthroplasty devices cleared through the Food and Drug Administration (FDA) 510(k)-notificati...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Cureus
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7489788/ https://www.ncbi.nlm.nih.gov/pubmed/32944459 http://dx.doi.org/10.7759/cureus.9744 |