Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K101997 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Numbe... | 2 | 12/01/2021 |
FEI # 3006179046 NuVasive Specialized Orthopedics, Inc. |
| NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System End Cap for PRECICE In... | 2 | 04/05/2021 |
FEI # 3006179046 Nuvasive Specialized Orthopedics Inc |
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