Arch Intern Med. 2010 Nov 8;170(20):1831-3. doi: 10.1001/archinternmed.2010.323. Epub 2010 Aug 9.

Medical devices and the FDA approval process: balancing safety and innovation; comment on "prevalence of fracture and fragment embolization of bard retrievable vena cava filters and clinical implications including cardiac perforation and tamponade".

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Department of Medicine, University of California, San Francisco, 505 Parnassus, M-1180, San Francisco, CA 94143-0124, USA. redberg@medicine.ucsf.edu

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Medical devices and the approval processes: United States vs France. [Arch Intern Med. 2010]
Medical devices and the approval processes: United States vs France.Braillon A. Arch Intern Med. 2010 Dec 13; 170(22):2040-1.

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Prevalence of fracture and fragment embolization of Bard retrievable vena cava filters and clinical implications including cardiac perforation and tamponade. [Arch Intern Med. 2010]
Prevalence of fracture and fragment embolization of Bard retrievable vena cava filters and clinical implications including cardiac perforation and tamponade.Nicholson W, Nicholson WJ, Tolerico P, Taylor B, Solomon S, Schryver T, McCullum K, Goldberg H, Mills J, Schuler B, et al. Arch Intern Med. 2010 Nov 8; 170(20):1827-31. Epub 2010 Aug 9.

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Prevalence of fracture and fragment embolization of Bard retrievable vena cava filters and clinical implications including cardiac perforation and tamponade. [Arch Intern Med. 2010]
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Medical devices and the FDA approval process: balancing safety and innovation; c...
Medical devices and the FDA approval process: balancing safety and innovation; comment on "prevalence of fracture and fragment embolization of bard retrievable vena cava filters and clinical implications including cardiac perforation and tamponade".
Arch Intern Med. 2010 Nov 8 ;170(20):1831-3. doi: 10.1001/archinternmed.2010.323. Epub 2010 Aug 9 .

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