Medical Device Recalls
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1 result found
510(K) Number: K950542 |
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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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Porous titanium flared rim acetabular shell with three clustered holes in even sizes from 48 to 66mm... | 3 | 04/27/2006 | Encore Medical, Lp |
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