Medical Device Recalls
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1 result found
510(K) Number: K971756 |
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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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Medtronic SPECIFY, 3998, Lead Kit for Spinal Cord Stimulation (SCS). Manufactured at Medtronic, Inc... | 2 | 09/18/2008 | Medtronic Neuromodulation |
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