Medical Device Recalls
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1 result found
510(K) Number: K101761 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ***REF 186-01-08***InteGrip ACETABULAR AUGMENT***SMALL 8mm. Use with 48/50mm Shell.***EXACTECH, Gain... | 2 | 02/03/2014 | Exactech, Inc. |
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