Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K020741 |
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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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EPIK® KNEE SYSTEM Angled Insert Impactor RM/LL; Part #801-03-052 Rev. A; non-sterile; knee prosthesi... | 2 | 10/10/2007 | Encore Medical, Lp |
EPIK® KNEE SYSTEM Angled Insert Impactor LM/RL; Catalog #801-03-051 Rev. A; non-sterile; knee prosth... | 2 | 10/10/2007 | Encore Medical, Lp |
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