Medical Device Recalls
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1 result found
510(K) Number: K100448 |
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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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Integra Titan Reverse Shoulder System right and left head cutting templates, 142.5 degrees. The R... | 2 | 11/08/2014 | Integra LifeSciences Corp. |
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