Medical Device Recalls
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510(K) Number: K031807 |
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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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Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usa... | 2 | 04/05/2016 | Synthes (USA) Products LLC |
Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usa... | 2 | 04/05/2016 | Synthes (USA) Products LLC |
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