Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K981075 |
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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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| TI Single Vector Distractor Body with Right Foot/20mm; Catalog ID 487.962 The Titanium Single Vec... | 2 | 08/17/2016 | Synthes (USA) Products LLC |
| TI Single Vector Distractor Body with Left Foot/20mm; Catalog ID 487.963 The Titanium Single Vect... | 2 | 08/17/2016 | Synthes (USA) Products LLC |
| TI Single Vector Distractor Proximal Foot/Left; Catalog ID 487.975 The Titanium Single Vector Dis... | 2 | 08/17/2016 | Synthes (USA) Products LLC |
| TI Single Vector Distractor Body with Left Foot/30mm; Catalog ID 487.965 The Titanium Single Vect... | 2 | 08/17/2016 | Synthes (USA) Products LLC |
| TI Single Vector Distractor Proximal Foot/Right; Catalog ID 487.974 The Titanium Single Vector Di... | 2 | 08/17/2016 | Synthes (USA) Products LLC |
| TI Single Vector Distractor Body with Right Foot/30mm; Catalog ID 487.964 The Titanium Single Vec... | 2 | 08/17/2016 | Synthes (USA) Products LLC |
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