Medical Device Recalls
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1 result found
510(K) Number: K863943 |
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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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| MEDPOR® Surgical Implant * POREX Surgical Products Group * Sterile/EO * Implant, Non-Pyrogenic, For ... | 3 | 04/16/2005 |
FEI # 1000131961 Porex Surgical, Inc. |
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