Materials and Methods
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- PMA P050053, original application.Accessed September 1, 2011)
- Accessed September 1, 2011)
- http://www.fda.gov/medicaldevices/deviceregulationandguidance/postmarketrequirements/reportingadverseevents/ucm127891.htm(Accessed September 1, 2011)
There was no external funding source. The author does not have any commercial association with the pharmaceutical industry. The views expressed in this article are the author's own and do not reflect the official policy or position of the US Food and Drug Administration.
This is a US government work. There are no restrictions on its use.