Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K936159 |
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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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Natural-Knee® N-K II DOMED ALL-POLY PAT, SZ0 N-K II DOMED ALL-POLY PAT, SZ1 | 2 | 03/20/2014 | Zimmer, Inc. |
Natural-Knee® II System: POLY ULTRA TIB LT SZ00/9M POLY ULTRA TIB LT SZ0/9MM POLY ULTRA TIB LT SZ... | 2 | 03/20/2014 | Zimmer, Inc. |
Natural-Knee® II Femoral Component | 2 | 10/25/2013 | Zimmer, Inc. |
Natural-Knee® Flex Femoral Component. Provides increased flexion capability. | 2 | 10/25/2013 | Zimmer, Inc. |
NP FEM LT SZ0 NATURAL-KNE NP FEM RT SZ0 NATURAL-KNE NP FEM LT SZ2 NATURAL-KNE NP FEM RT SZ2 NATUR... | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
NKII CSTI Porous Femoral NKII NP Femoral prosthesis, knee, patellofemorotibial, semi-constrained, ... | 2 | 02/22/2016 | Zimmer Biomet, Inc. |
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