Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K031585 |
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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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Optima Spinal System and Spinal Hook System, set screw component. | 2 | 09/08/2004 | U&I America |
2.5mm Hex Driver | 2 | 02/27/2004 | U&I America |
4mm Hex Driver | 2 | 02/27/2004 | U&I America |
Optima Poly Screw Driver. | 2 | 08/27/2003 | U&I America |
Optima Large Poly Screw Driver | 2 | 08/27/2003 | U&I America |
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