Medical Device Recalls
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1 result found
510(K) Number: K023243 |
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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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Prot®g® Self-Expanding Nitinol Stent 6 mm x 40 mm, Model Number SER6-6-40-135 | 3 | 05/22/2003 | ev3, Inc. |
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