Medical Device Recalls
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1 result found
510(K) Number: K163634 |
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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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SOUTHERN IMPLANTS REF IBR12d-13, Implant, Ext. Hex, tapered 12o Co-Axis(TM) intended for surgical pl... | 2 | 04/16/2018 | Southern Implants, (Pty.) Ltd. |
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