Medical Device Recalls
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1 result found
510(K) Number: K090064 |
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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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Copperhead IBFD, Large Neutral, 6mm Copperhead IBFD, Large Neutral, 7mm Copperhead IBFD, Large N... | 2 | 05/27/2013 | Spinal Solutions, LLC |
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