Medical Device Recalls
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1 result found
510(K) Number: K122985 |
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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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Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7 | 2 | 12/13/2013 | Aesculap, Inc. |
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