Medical Device Recalls
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1 result found
510(K) Number: K935137 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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TefGen is an implant material which is intended to be used as a temporary space-making barrier over ... | 3 | 07/20/2004 | Lifecore Biomedical, Inc. |
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