Medical Device Recalls
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1 result found
510(K) Number: K192049 |
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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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Oryx Cervical Screw Caddy, Model Number BTA-172, as part of the Oryx Cervical Plate System - Product... | 2 | 05/20/2020 | Innovasis, Inc |
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