Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K123705 |
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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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| Trinity Acetabular System Product Usage - Total Hip Replacement. | 2 | 04/22/2016 |
FEI # 1000131827 Corin USA Limited |
| Trinity Acetabular Shell Product Usage: Total Hip Replacement. | 2 | 04/22/2016 |
FEI # 1000131827 Corin USA Limited |
| Trinity Acetabular Shell Product Usage Total Hip Replacement. | 2 | 04/22/2016 |
FEI # 1000131827 Corin USA Limited |
| Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, ... | 2 | 09/30/2021 |
FEI # 3002806725 Corin Ltd |
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