Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K031595 |
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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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| Optima Spinal System and Spinal Hook System, set screw component. | 2 | 09/08/2004 | U&I America |
| 4mm Hex Driver | 2 | 02/27/2004 | U&I America |
| 2.5mm Hex Driver | 2 | 02/27/2004 | U&I America |
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