Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K051611 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Integra bioBLOCK Resorbable subtaler Implant, 12mm Catalog Number: 040012 - Product Usage: The bi... | 2 | 04/05/2019 |
FEI # 3001700044 Integra Limited |
| Integra bioBLOCK Resorbable subtaler Implant, 11mm Catalog Number: 040011 - Product Usage: The bi... | 2 | 04/05/2019 |
FEI # 3001700044 Integra Limited |
| Integra bioBLOCK Resorbable subtaler Implant, 10mm Catalog Number: 40010 - Product Usage: The bio... | 2 | 04/05/2019 |
FEI # 3001700044 Integra Limited |
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