Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K973412 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. ... | 2 | 07/01/2015 | Zimmer, Inc. |
| Natural-Knee® II Constrained Knee System NKII CCK TIB INS SZ00/0-L NKII CCK TIB INS SZ1/2-LF NKII... | 2 | 03/20/2014 | Zimmer, Inc. |
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