טוען...
Improving the Postmarket Surveillance of Total Joint Arthroplasty Devices
OBJECTIVE: To evaluate the FDA’s approval process and postmarket surveillance strategies for THR devices. DESIGN: The FDA Center for Devices and Radiological Health (CDRH) 510k releasable database was used to document approved THR devices. The CDRH Medical Device Reporting data files were used to st...
שמור ב:
| Main Authors: | , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Bentham Science Publishers Ltd.
2008
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2577946/ https://ncbi.nlm.nih.gov/pubmed/19088864 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1874312900802010007 |
| תגים: |
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