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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K800894
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 5, Sterile, DePuy Orthopaedics. This dev... 2 03/17/2011 FEI # 1818910
Depuy Orthopaedics, Inc.
DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 5, Sterile, DePuy Orthopaedics. This de... 2 03/17/2011 FEI # 1818910
Depuy Orthopaedics, Inc.
DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 4, Sterile, DePuy Orthopaedics. This dev... 2 03/17/2011 FEI # 1818910
Depuy Orthopaedics, Inc.
DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 3, Sterile, DePuy Orthopaedics. This de... 2 03/17/2011 FEI # 1818910
Depuy Orthopaedics, Inc.
DePuy, a Johnson & Johnson company, CEMENT RESTRICTOR, Size 1, Sterile, DePuy Orthopaedics. This dev... 2 03/17/2011 FEI # 1818910
Depuy Orthopaedics, Inc.
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