Medical Device Recalls
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1 result found
510(K) Number: K122011 |
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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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The Brainlab Offset Cup Impactor Universal. Part of the Brainlab hip system. An intraoperative im... | 2 | 02/26/2015 | Brainlab AG |
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