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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K904880
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Endotec Prosthesis Shoulder, Titanium Alloy, Sterilized Modular Femoral Stem BP Shoulder Componen... 2 05/20/2010 FEI # 3004553437
Endotec, Inc.
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