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THE STRYKER FAILURE TIMELINE April 14, 2008 June 3, 2008 Stryker submits the stryker Rejuvenate Modular Hip system's 501(k) to the FDA The FDA approves the application, based on a determination that the Stryker Rejuvenate was substantially similar to an existing product. August 21, 2009 Stryker submits the Stryker ABG II Modular-Neck Stem's 501(k) to the FDA October, 2009 The FDA approves the application, based on a determination that the Stryker ABG IIl was substantially February 2010 similar to an existing product. Stryker begins marketing the Rejuvenate Modular Primary Hip System to doctors and medical facilities April 2012 July 6, 2012 Stryker issues an "Urgent Safety Alert" informing doctors of the potential side effects of using the Rejuvenate system. Stryker issues a voluntary recall of all Rejuvenate and ABG II devices sold in the United States. A voluntary recall means it was issued by the manufacturer, though most recalls are also done with the help and cooperation of the FDA. RECALL DANGEROUS SIDE EFFECTS

Infographic Presentation

shared by PitchWorx on Jan 12
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Infographic based presentation designed for a medical attorney.

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