Cobalt Poisoning From Hips: Stryker Rejuvenate Received 510k FDA Approval as Opposed to Full PMA Approval

Although the Rejuvenate was approved in 2008, it was done through an FDA process known as the 510(k) which is more a clearance than an actual approval. This type of clearance is granted based on the fact that the device is substantially equivalent to a device already on the market.
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Chromium and Cobalt Poisoning Seen in Pinnacle

Although the recalled DePuy ASR metal-on-metal hip implant has repeatedly made the news regarding the risk of metal poisoning from the friction of the metal parts which then release cobalt and chromium ions into the bloodstream and surrounding tissues, it is likely that the Pinnacle implant shares the same risks.
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Chromium Poisoning Just as Dangerous as Cobalt Poisoning

Early this year, DePuy issued their recall for the ASR XL Acetabular System sold in the United States. Doctors began recommending revision surgery to those of their patients who reported pain or an overall failure of the DePuy hip implant.
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