Medical Device Recalls
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1 result found
510(K) Number: K070460 |
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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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Allez Spine Cross Connectors; Catalog Number: LG-CC1001Cross Link, Small 30-37mm; LG-CC1002 Cross Li... | 2 | 10/28/2008 | Allez Spine, LLC |
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