Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K170613 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Genius Knee Cemented Tibial Component Product Usage: Knee replacement component | 2 | 02/14/2019 |
FEI # 3008262872 Signature Orthopedics Pty Limited |
| Genius Knee Cemented CR Femoral Component Product Usage: Knee replacement component | 2 | 02/14/2019 |
FEI # 3008262872 Signature Orthopedics Pty Limited |
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