Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K082332 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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5.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP, KWQ, MNH, MNI | 2 | 11/19/2012 | NuVasive Inc |
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