Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K962152 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Scorpio Total Knee Posteriorly Stabilized Femoral Component, #7R, Catalog No.: 71-4107R, Lot Code: K... | 2 | 09/11/2008 | Stryker Howmedica Osteonics Corp. |
Scorpio Total Knee Posteriorly Stabilized Femoral Component; Knee joint patellofemorotibial polymer/... | 3 | 07/16/2008 | Stryker Howmedica Osteonics Corp. |
Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker... | 2 | 05/19/2015 | Stryker Howmedica Osteonics Corp. |
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