Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K061067 |
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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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Trabecular Metal acetabular revision system buttress augment size, 54, 00-4898-001-54, sterile, Zimm... | 2 | 08/12/2010 | Zimmer Inc. |
Trabecular Metal acetabular revision system column buttress right posterior/left anterior, 00-4894... | 2 | 08/12/2010 | Zimmer Inc. |
Trabecular Metal acetabular revision system column buttress left posterior/right anterior, 00-4894-3... | 2 | 08/12/2010 | Zimmer Inc. |
Trabecular Metal acetabular revision system buttress augment size, 58, 00-4898-001-58, sterile, Zimm... | 2 | 08/12/2010 | Zimmer Inc. |
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