Medical Device Recalls
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1 result found
510(K) Number: K081653 |
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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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MDI Hybrid Implant, O-Ball abutment, sizes 2.9mm x 13mm and 2.9mm x 15mm, endosseous dental implant.... | 2 | 09/10/2009 | IMTEC Corporation |
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