Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K061813 |
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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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Stryker Mantis Rod Inserter Inner Shaft; Non Sterile; Manufactured by Stryker Spine SAS, Cestas Fran... | 2 | 07/07/2009 | Stryker Spine |
Stryker Mantis Rod Inserter; Non Sterile, Manufactured by Stryker Spine SAS, Cestas, France. Distri... | 2 | 07/07/2009 | Stryker Spine |
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