Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K120906 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| TM Ankle and Ankle Talus L/R, Item Nos. 00450001100 00450001200 00450001300 00450001400 00450001... | 2 | 11/07/2019 |
FEI # 1000220733 Zimmer Biomet, Inc. |
| Zimmer Trabecular Metal Total Ankle Tibial Base Component Sizes 1-6 Total ankle arthroplasty is ... | 2 | 12/10/2013 |
FEI # 1000220733 Zimmer, Inc. |
| Zimmer Trabecular Metal Total Ankle Talar Component Left Sizes 1-6 Total ankle arthroplasty is in... | 2 | 12/10/2013 |
FEI # 1000220733 Zimmer, Inc. |
| Zimmer Trabecular Metal Total Ankle Talar Component Right Sizes 1-6 Total ankle arthroplasty is i... | 2 | 12/10/2013 |
FEI # 1000220733 Zimmer, Inc. |
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