Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K150481 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2 Lumbar implants are in... | 2 | 06/01/2021 | K2M, Inc |
| Cascadia AN Interbody Convex 10x28x14mm Catalog Number: 6101-2102814NC-G2 Lumbar implants are ... | 2 | 06/01/2021 | K2M, Inc |
| Cascadia AN Interbody Convex 10x22x15mm Catalog Number: 6101-2102215NC-G2 Lumbar implants are ... | 2 | 06/01/2021 | K2M, Inc |
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