Medical Device Recalls
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1 result found
510(K) Number: K120115 |
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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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Orthosize Templating Version 1.2.6 Echo Bi-Metric Hip Stem Digital Templates. For preoperative plan... | 2 | 03/13/2017 | Zimmer Biomet, Inc. |
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