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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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Detalles Bibliográficos
Autores principales: Pellerin, Carl, Adamson, Micah, Janney, Cory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
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