Medical Device Recalls
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1 result found
510(K) Number: K042598 |
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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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Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58 mm Length; Zimmer Periarticular Lo... | 2 | 01/13/2016 | Zimmer Biomet, Inc. |
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