Medical Device Recalls
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1 result found
510(K) Number: K063333 |
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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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MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical ... | 2 | 12/12/2012 | Siemens Medical Solutions USA, Inc |
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