Medical Device Recalls
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1 result found
510(K) Number: K143517 |
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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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| Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: The Applied Voyant Open Fusio... | 2 | 09/15/2015 |
FEI # 2027111 Applied Medical Resources Corp |
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