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The First 18 Months Following Food and Drug Administration Approval of Lumbar Total Disc Replacement in the United States: Reported Adverse Events Outside an Investigational Device Exemption Study Environment
BACKGROUND: Introduction of a new surgical technology may result in higher rates of adverse events compared with rates reported in the study performed to gain regulatory approval. The purpose of our study was to describe the incidence of reported adverse events during the first 18 months following U...
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| Gepubliceerd in: | SAS J |
|---|---|
| Hoofdauteurs: | , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
RRY Publications, LLC
2007
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4365565/ https://ncbi.nlm.nih.gov/pubmed/25802573 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/SASJ-2006-0001-RR |
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