Medical Device Recalls
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1 result found
510(K) Number: K123461 |
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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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StaXx® IB Convex Expandable Implant (25 x 12 x 9 mm), Intervertebral Fusion Device, Lumbar; Catalog ... | 2 | 09/11/2013 | Spine Wave, Inc. |
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