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PUBMED FOR HANDHELDS

Journal Abstract Search


641 related items for PubMed ID: 21321283

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  • 2. Assessment of cardiovascular and noncardiovascular medical device recalls.
    Somberg JC, McEwen P, Molnar J.
    Am J Cardiol; 2014 Jun 01; 113(11):1899-903. PubMed ID: 24837271
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  • 4. How do Orthopaedic Devices Change After Their Initial FDA Premarket Approval?
    Samuel AM, Rathi VK, Grauer JN, Ross JS.
    Clin Orthop Relat Res; 2016 Apr 01; 474(4):1053-68. PubMed ID: 26584802
    [Abstract] [Full Text] [Related]

  • 5. Analysis of FDA-Approved Orthopaedic Devices and Their Recalls.
    Day CS, Park DJ, Rozenshteyn FS, Owusu-Sarpong N, Gonzalez A.
    J Bone Joint Surg Am; 2016 Mar 16; 98(6):517-24. PubMed ID: 26984921
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  • 6. Medical device recalls: get it right the first time: Comment on "Medical device recalls and the FDA approval process".
    Redberg RF, Dhruva SS.
    Arch Intern Med; 2011 Jun 13; 171(11):1011-2. PubMed ID: 21321286
    [No Abstract] [Full Text] [Related]

  • 7. Research: Evaluation of Orthopedic Hip Device Recalls by the FDA from 2007 to 2017.
    Peters W, Pellerin C, Janney C.
    Biomed Instrum Technol; 2020 Nov 01; 54(6):418-426. PubMed ID: 33339030
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  • 8. Risk of Recall Among Medical Devices Undergoing US Food and Drug Administration 510(k) Clearance and Premarket Approval, 2008-2017.
    Dubin JR, Simon SD, Norrell K, Perera J, Gowen J, Cil A.
    JAMA Netw Open; 2021 May 03; 4(5):e217274. PubMed ID: 33956132
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  • 9. Association Between Regulatory Submission Characteristics and Recalls of Medical Devices Receiving 510(k) Clearance.
    Everhart AO, Sen S, Stern AD, Zhu Y, Karaca-Mandic P.
    JAMA; 2023 Jan 10; 329(2):144-156. PubMed ID: 36625811
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  • 14. Mapping the genealogy of medical device predicates in the United States.
    Pai DB.
    PLoS One; 2021 Jan 10; 16(10):e0258153. PubMed ID: 34618861
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  • 17. FDA recalls not as alarming as they seem.
    Connor JT, Lewis RJ, Berry DA, Berry SM.
    Arch Intern Med; 2011 Jun 13; 171(11):1044-5; author reply 1045-6. PubMed ID: 21670380
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  • 18. Export of pharmaceuticals and medical devices under the federal Food, Drug & Cosmetic Act: FDA's striking change in interpretation post-Shelhigh.
    Basile EM, Tolomeo D, Gluck E.
    Food Drug Law J; 2009 Jun 13; 64(1):149-69. PubMed ID: 19998744
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