Medical Device Recalls
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1 result found
510(K) Number: K061410 |
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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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| Zimmer Dental AdVent Implant System, Abutment, Tapered, Rx, sterile, Zimmer Dental, Inc., Carlsbad, ... | 2 | 12/10/2009 |
FEI # 1000220733 Zimmer Inc. |
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