Medical Device Recalls
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1 result found
510(K) Number: K032812 |
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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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Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard Endoskeleton Implant VBR ... | 2 | 12/17/2012 | TITAN SPINE, LLC |
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