Medical Device Recalls
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1 result found
510(K) Number: K183060 |
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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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CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 40mm Material Number: 66-240 - Product U... | 2 | 03/11/2021 | RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.) |
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