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An Analysis of Foot and Ankle Device Recalls by the Food and Drug Administration
Introduction Orthopaedic devices represent 12% of all medical device recalls. Products are approved through pre-market approval (PMA) or the 510(k) premarket notification process. No previous evaluation was found in the literature evaluating foot and ankle device recalls. The field of foot and ankle...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177061/ https://www.ncbi.nlm.nih.gov/pubmed/30338198 http://dx.doi.org/10.7759/cureus.3123 |