Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K021458 |
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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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Synthes In Situ Bender/Cutter Kit-Wide-Sterile. Catalog Number 530.521S. | 2 | 02/24/2010 | Synthes USA (HQ), Inc. |
Synthes InSitu Bender Cutter Kit Wide Sterile Catalog number 530.521S, used with Synthes Rapid Resor... | 2 | 06/01/2009 | Synthes Spine |
Synthes InSitu Bender Cutter Kit Narrow Sterile Catalog number 530.522S, used with Synthes Rapid Res... | 2 | 06/01/2009 | Synthes Spine |
In Situ Bender Cutter Kit Wide Sterile, Catalog number 530.521S Used with Synthes' Rapid Resorbab... | 2 | 05/21/2009 | Synthes Spine |
In Situ Bender Cutter Kit Narrow Sterile, Catalog number 530.522S. Used with Synthes' Rapid Resor... | 2 | 05/21/2009 | Synthes Spine |
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