Medical Device Recalls
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1 result found
510(K) Number: K031855 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| TraXis Vue Spinal Implant System, Part #2601-090921 | 2 | 02/07/2006 |
FEI # 3000718496 Abbott Spine |
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