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Recent Device Approvals: Prestige LP Cervical Disc

The U.S. Food and Drug Administration has recently approved the Prestige LP Cervical Disc to be marketed.  The Prestige LP Cervical Disc treats one diseased disc in the neck (cervical disc) that causes arm pain and/or weakness or numbness (radiculopathy or myelopathy). The Prestige LP Cervical Disc consists of a titanium-ceramic alloy that fits between the top and bottom surface of the neck bones (cervical vertebrae).  For more information, please see: http://www.fda.gov/MedicalDevices/ProductsandMedicalProcedures/DeviceApprovalsandClearances/Recently-ApprovedDevices/ucm408505.htm


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