Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-0124-2017 - Calix P PEEK Lumbar System, PLIF Rasp | 2 | 10/18/2016 |
FEI # 3005031160 X Spine Systems Inc |
| Z-0125-2017 - Calix P PEEK Lumbar System, PLIF Trial | 2 | 10/18/2016 |
FEI # 3005031160 X Spine Systems Inc |
| Z-0126-2017 - Calix T PEEK Lumbar System, TLIF Rasp | 2 | 10/18/2016 |
FEI # 3005031160 X Spine Systems Inc |
| Z-0127-2017 - Calix T PEEK Lumbar System, TLIF Trial | 2 | 10/18/2016 |
FEI # 3005031160 X Spine Systems Inc |
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