Medical Device Recalls
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1 result found
510(K) Number: K130380 |
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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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Verasense Knee System, Model SYK-TRCR 02. Intelligent disposable tibial insert that measures dynami... | 2 | 01/29/2015 | Orthosensor, Inc. |
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