Medical Device Recalls
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1 result found
510(K) Number: K002897 |
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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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Universal Titanium Prosthesis, Round Head, with Flex H/A titanium shoe. The ear prosthesis is implan... | 2 | 09/26/2013 | Medtronic Xomed, Inc. |
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