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  2. Derek McMinn - Wikipedia

    en.wikipedia.org/wiki/Derek_McMinn

    McMinn first began performing hip resurfacing procedures in 1991 using the McMinn Resurfacing, manufactured by Corin. [2] The rationale behind the procedure was that it would be a bone-conserving alternative to THR for patients with higher activity demands i.e. young patients with severe hip arthritis who are otherwise in good health.

  3. Talk:Hip resurfacing - Wikipedia

    en.wikipedia.org/wiki/Talk:Hip_resurfacing

    Here are links to possibly useful sources of information about Hip resurfacing. PubMed provides review articles from the past five years (limit to free review articles)

  4. Metallosis - Wikipedia

    en.wikipedia.org/wiki/Metallosis

    In August 2010, DePuy recalled its hip replacement systems ASR XL Acetabular Hip Replacement System and ASR Hip Resurfacing System due to failure rates and side effects including metallosis. The recalls triggered a large number of lawsuits against DePuy and its parent company Johnson & Johnson upon claims that the companies knew about the ...

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    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  6. Femoral neck targeting - Wikipedia

    en.wikipedia.org/wiki/Femoral_neck_targeting

    In hip resurfacing surgery, accurately identifying the true centre of the femoral neck in both antero-posterior (AP) and lateral planes is crucial. This reference point is essential for the precise positioning of the femoral neck. Failure to correctly position the femoral component can lead to early implant failure.

  7. 2010 DePuy Hip Recall - Wikipedia

    en.wikipedia.org/wiki/2010_DePuy_Hip_Recall

    Medical Device Alert: DePuy ASR TM acetabular cups used in hip resurfacing arthroplasty and total hip replacement, Medicines and Healthcare products Regulatory Agency, MDA/2010/044, 25 May 2010; Medical Device Alert: All metal-on-metal (MoM) hip replacements, Medicines and Healthcare products Regulatory Agency, MDA/2012/008, 28 February 2012

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