Medical Device Recalls
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11 to 13 of 13 Results
510(K) Number: K962152 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Scorpio PS Femur Waffle Posts with LfIt; Stryker Orthopaedics, 325 Corporate Drive, Mahwah, NJ 0743... | 2 | 12/01/2009 | Stryker Howmedica Osteonics Corp. |
| Osteonics Scorpio Total Knee; Posteriorly Stabilized Femoral Component; #13 with posts, low frict... | 2 | 09/16/2008 | Stryker Howmedica Osteonics Corp. |
| Scorpio Total Knee Posteriorly Stabilized Femoral Component, #7R, Catalog No.: 71-4107R, Lot Code: K... | 2 | 09/11/2008 | Stryker Howmedica Osteonics Corp. |
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