Medical Device Recalls
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1 result found
510(K) Number: K120493 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth ga... | 2 | 09/22/2014 | Instratek, Incorporated |
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