Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K153340 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Epic Extremity Plate System,10x10 Plate Caddy, Part 2111-1010 with 2.7 and 3.5mm Non-Locking Screw (... | 2 | 05/15/2018 |
FEI # 3012453147 Epic Extremity, LLC |
| Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (... | 2 | 05/15/2018 |
FEI # 3012453147 Epic Extremity, LLC |
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