Medical Device Recalls
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1 result found
510(K) Number: K954555 |
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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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VERSA-FX II KEYLESS TUBE, VERSA-FX II KEYLESS SHORT, VERSA-FX II SHORT TUBE PL, VERSA-FX II STD TUBE... | 2 | 02/20/2014 | Zimmer, Inc. |
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