Medical Device Recalls
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1 result found
510(K) Number: K001238 |
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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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HT X-DRIVE SCREW, Part # 91-2416, W.Lorenz Surgical. Screws for use in the stabilization and fixat... | 2 | 11/04/2008 | Biomet Microfixation, Inc. |
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