Medical Device Recalls
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1 result found
510(K) Number: K120241 |
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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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djosurgical Linear Neck Trials with Spring Sides, Standard, nonsterile, REF S-200635; and djosurgica... | 2 | 04/10/2020 | Encore Medical, LP |
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