An evaluation of the Manufacturer And User Facility Device Experience database that inspired the United States Food and Drug Administration's Reclassification of transvaginal mesh
2018 ◽
Vol 59
(2)
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pp. 126
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Keyword(s):
2000 ◽
Vol 1495
(2)
◽
pp. 150-159
◽
2015 ◽
Vol 115
(1)
◽
pp. 95-100
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Keyword(s):
Keyword(s):
Keyword(s):