Medical Device Recalls
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1 result found
510(K) Number: K951740 |
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Results per Page |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| The Polarus Plus Humeral Rod (part number HR-0824-S) is intended as an intramedullary fixation devic... | 2 | 04/02/2012 |
FEI # 1000125930 Acumed LLC |
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