Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K141739 |
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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 | NuVasive Specialized Orthopedics, Inc. |
| NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System Implant; Packaged E... | 2 | 04/05/2021 | Nuvasive Specialized Orthopedics Inc |
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