Medical Device Recalls
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1 result found
510(K) Number: K990622 |
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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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BOLD/INI-CLIP 2.2mm Drill Bit with AO Attachment. | 2 | 01/09/2007 | Integra LifeSciences Corp. |
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