Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K002639 |
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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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Depuy Mitek Bioknotless Anchor with Panacryl Suture Ref No. 212729 | 3 | 03/15/2006 | Depuy Mitek, a Johnson & Johnson Co. |
Depuy Mitek Bioknotless Anchor with Ethibond Suture Ref No. 212728 | 3 | 03/15/2006 | Depuy Mitek, a Johnson & Johnson Co. |
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