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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K120906
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Product Description
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Recall
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FDA Recall
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TM Ankle and Ankle Talus L/R, Item Nos. 00450001100 00450001200 00450001300 00450001400 00450001... 2 11/07/2019 Zimmer Biomet, Inc.
Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Total ankle arthroplasty is ... 2 12/10/2013 Zimmer, Inc.
Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is in... 2 12/10/2013 Zimmer, Inc.
Zimmer Trabecular Metal Total Ankle Talar Component Right Sizes 1-6 Total ankle arthroplasty is i... 2 12/10/2013 Zimmer, Inc.
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