Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K173736 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base ... | 2 | 02/09/2023 |
FEI # 3014391847 Trackx Technology Inc |
| Product Name: Insight Base Flex - 8, Ref 608-3TX; The device consists of a sterile Snap that include... | 3 | 10/30/2024 |
FEI # 3014391847 Trackx Technology Inc |
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