Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K833921 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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AGC 2000 LP Patella, labeled as AGC Porous Patellar Med, Model Number 150804. Product Usage: For... | 2 | 02/15/2018 | Zimmer Biomet, Inc. |
AGC 2000 LP Patella, labeled as AGC Porous Patellar SM, Model Number 150802. Product Usage: For ... | 2 | 02/15/2018 | Zimmer Biomet, Inc. |
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