Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K060271 |
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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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| SpiraLok 5.0mm with Panacryl and needles Product Number: 222961 SPIRALOK Anchors are primarily u... | 2 | 10/25/2012 |
FEI # 1221934 DePuy Mitek, Inc., a Johnson & Johnson Co. |
| SpiraLok 5.0mm with Ethibond and needles Product Number: 222960 SPIRALOK Anchors are primarily u... | 2 | 10/25/2012 |
FEI # 1221934 DePuy Mitek, Inc., a Johnson & Johnson Co. |
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