Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K101030 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| K-Wire HBS Sterile Lot, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw sys... | 2 | 08/12/2019 |
FEI # 1832656 BioPro, Inc. |
| K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system ... | 2 | 08/12/2019 |
FEI # 1832656 BioPro, Inc. |
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