Medical Device Recalls
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1 result found
510(K) Number: K042271 |
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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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NexGen Complete Knee Solution Stemmed tibial broach impactor, Catalog # 00-5977-011-00, Zimmer Inc.,... | 2 | 12/13/2010 | Zimmer Inc. |
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