Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060156 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| I.T.S. Screw System with the below descriptions and corresponding article numbers. 1. Cancellous... | 2 | 03/20/2026 |
FEI # 3004369035 I.T.S. GmbH |
| I.T.S. Straight Plate with Angular Stability with the below descriptions and corresponding article n... | 2 | 03/20/2026 |
FEI # 3004369035 I.T.S. GmbH |
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