Medical Device Recalls
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1 result found
510(K) Number: K123604 |
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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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Stryker, T2 Guidewire, Ball-Tipped, 3x800 mm Product Usage: Intended for the temporary stabiliza... | 2 | 02/25/2016 | Stryker Howmedica Osteonics Corp. |
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