Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K971247 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Passive Biopsy Needle Kit, UDI: 00643169030121 and 00643169702943 | 2 | 12/06/2019 | Medtronic Navigation, Inc. |
Biopsy Needle FPU Kit, Product # 9731754, UDI: 00643169341517 | 2 | 12/06/2019 | Medtronic Navigation, Inc. |
Biopsy Needle FPU Kit, Product # 9736075, UDI: 00763000063108 | 2 | 12/06/2019 | Medtronic Navigation, Inc. |
Medtronic Passive Biopsy Needle Kit, Part Number 9733068 - Passive Biopsy Needle Kit. The image g... | 2 | 08/03/2015 | Medtronic Navigation, Inc. |
Medtronic Passive Biopsy Needle Kit, Part Number 9731754 - Passive Biopsy Fee Per Use (FPU) Kit. ... | 2 | 08/03/2015 | Medtronic Navigation, Inc. |
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