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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...
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| Publicado no: | Cureus |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cureus
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7489788/ https://ncbi.nlm.nih.gov/pubmed/32944459 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.9744 |
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