Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K071914 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Mercury Spinal System DIA 5.5 x 30 MM Lordosed Rod, Part Number: 60100-030. Intended to provide... | 3 | 05/07/2013 |
FEI # 3004893332 Spinal Elements, Inc |
| Mercury Spinal System DIA 5.5 x 40 MM Lordosed Rod, Part Number: 60100-040. Intended to provide... | 3 | 05/07/2013 |
FEI # 3004893332 Spinal Elements, Inc |
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