Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K920034 |
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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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Duracon Total Knee Distal Femoral Locking Screw for 5 mm Spacer; Product No. 6632-5-600. Made in ... | 2 | 10/06/2010 | Stryker Howmedica Osteonics Corp. |
Duracon Total Knee Modular Femoral Component; Non-Porous Right Medium Assembly, Product No. 6632-0-... | 3 | 09/21/2007 | Stryker Howmedica Osteonics Corp. |
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