Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K953268 |
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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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Dual Taper Wedge Pressed Fit Femoral Component. The Dual Taper Wedge is a single use device inten... | 2 | 03/31/2009 | Stelkast Co |
Stelkast Dual Taper Wedge Pressed Fit Femoral Component. Hip Prosthesis, Part number SC1439 | 2 | 01/28/2009 | Stelkast Co |
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