טוען...
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...
שמור ב:
| הוצא לאור ב: | Cureus |
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| Main Authors: | , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Cureus
2018
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| נושאים: | |
| גישה מקוונת: | 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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