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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 14 of 14 Results
510(K) Number: K960658
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Product Description
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FDA Recall
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CPT 12/14 COCR SIZE 1 EXT prosthesis, hip, semi-constrained, metal/polymer, porous uncemented 2 03/14/2018 Zimmer Biomet, Inc.
CPT 12/14 COCR SIZE 2 EXT prosthesis, hip, semi-constrained, metal/polymer, porous uncemented 2 03/14/2018 Zimmer Biomet, Inc.
CPT 12/14 COCR SIZE 2 STD prosthesis, hip, semi-constrained, metal/polymer, porous uncemented 2 03/14/2018 Zimmer Biomet, Inc.
CPT 12/14 COCR prosthesis, hip, semi-constrained, metal/polymer, porous uncemented various sizes ... 2 02/22/2016 Zimmer Biomet, Inc.
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