Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K050966 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ortho Development Corp., Pivot BiPolar Head, 28mm, Hip Prosthesis, Femoral Head. | 2 | 10/28/2009 | Ortho Development Corporation |
| Pivot Bipolar Cup 22x42/43-51/53mm, REF 133-YYYY Product Usage: Used in a hemiarthroplasty proce... | 2 | 08/17/2014 | Ortho Development Corporation |
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