Medical Device Recalls
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1 result found
510(K) Number: K090705 |
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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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Tibila Insert UC, Balanced Knee System, REF163-3YYY Product Usage: UHMWPE component used in TKA ... | 2 | 08/17/2014 | Ortho Development Corporation |
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