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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K934765
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Product Description
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FDA Recall
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TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O TRILOGY ACET SHELL 40MM O TRILOGY ACET SHELL ... 2 02/20/2014 Zimmer, Inc.
Trilogy Acetabular Shell Spiked. The Trilogy Acetabular System is indicated for either cemented o... 2 02/04/2013 Zimmer, Inc.
Trilogy Acetabular Shell with Cluster Holes. The Trilogy Acetabular System is indicated for eithe... 2 02/04/2013 Zimmer, Inc.
Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is indicated for either cemen... 2 02/04/2013 Zimmer, Inc.
Trilogy F/M Acetabular Shell without holes. Several ODs: 40MM, 42MM, 44MM, 46MM, 48MM, 50MM, 52MM, ... 2 02/04/2013 Zimmer, Inc.
Trilogy F/M Acetabular Shell with Uni-Hole. The Trilogy Acetabular System is indicated for either... 2 02/04/2013 Zimmer, Inc.
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