Medical Device Recalls
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11 to 11 of 11 Results
Related Medical Device Recalls Recall Date to: 10/09/2015 |
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Product Description
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Recall
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FDA Recall
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Z-0118-2010 - Synthes USA, TI Synex (TM) II Central Body 97mm - 123mm, Catalog number 04.808.011. Intended for use in the thoracolumbar spine (T1-L5) to replace a collapsed, damaged, or unstable vertebral body d... | 1 | 11/09/2009 | Synthes USA (HQ), Inc. |
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