Medical Device Recalls
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1 result found
510(K) Number: K102090 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| VisuALIF,System consisting of a 'U' shaped PEEK block in two footprint configurations, four heights ... | 2 | 09/19/2013 |
FEI # 3010266937 Spine Smith Holdings, LLC |
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