Medical Device Recalls
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1 result found
510(K) Number: K040415 |
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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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PSD Gel that's provided with Peri-Strips Dry Staple Line Reinforcement with Apex Processing (PSD) an... | 2 | 09/21/2010 | Synovis Surgical Inovation Div. of |
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