Medical Device Recalls
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1 result found
510(K) Number: K100089 |
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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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Synthes Spine T-PAL Spacer System. Transforaminal posterior atraumatic lumbar spacer system. Tra... | 2 | 11/04/2011 | Synthes USA (HQ), Inc. |
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