Medical Device Recalls
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1 result found
510(K) Number: K955271 |
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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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Microseal Augmented (20 degrees) Liner, acetabular liner component made from UHMW polyethylene (ASTM... | 2 | 10/22/2014 | Signal Medical Corporation |
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