Medical Device Recalls
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1 result found
510(K) Number: K140123 |
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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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| Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw sys... | 2 | 12/15/2020 | Zimmer Biomet, Inc. |
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