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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...
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| Publicat a: | Cureus |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Cureus
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6177061/ https://ncbi.nlm.nih.gov/pubmed/30338198 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.3123 |
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