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  2. 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

  3. Hip replacement - Wikipedia

    en.wikipedia.org/wiki/Hip_replacement

    Hip replacement is a surgical procedure in which the hip joint is replaced by a prosthetic implant, that is, a hip prosthesis. Hip replacement surgery can be performed as a total replacement or a hemi/semi (half) replacement. Such joint replacement orthopaedic surgery is generally conducted to relieve arthritis pain or in some hip fractures.

  4. DePuy Synthes - Wikipedia

    en.wikipedia.org/wiki/DePuy_Synthes

    On August 24, 2010, DePuy recalled all ASR hip implant systems sold since 2003. The 2010 DePuy Hip Recall was issued after research released by the National Joint Registry (NJR) found high rates of hip replacement failure for the ASR XL Acetabular and ASR Hip Resurfacing systems.

  5. Hip resurfacing - Wikipedia

    en.wikipedia.org/wiki/Hip_resurfacing

    Hip resurfacing has been developed as a surgical alternative to total hip replacement (THR). The procedure consists of placing a cap (usually made of cobalt-chrome metal), which is hollow and shaped like a mushroom, over the head of the femur while a matching metal cup (similar to what is used with a THR) is placed in the acetabulum (pelvis socket), replacing the articulating surfaces of the ...

  6. Hip, knee replacements back on track, boosting device makers

    www.aol.com/news/hip-knee-replacements-back...

    Older adults are catching up on missed hip and knee replacements and other non-urgent surgeries, a shift that will benefit medical device makers this year, Wall Street analysts said after insurer ...

  7. US FDA identifies recall of Philips medical imaging devices ...

    www.aol.com/news/us-fda-identifies-recall...

    The Dutch medical devices maker started the recall process on Nov. 30 this year and has recalled 150 devices in the United States. In the United States, customers with operational systems have ...