Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K030055 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma... | 3 | 06/11/2015 |
FEI # 1825034 Biomet, Inc. |
| Mallory Head 4 Finned Acetabular Shell 50 mm, PN 13-104150, hip prosthesis component (Ringloc) | 2 | 02/17/2015 |
FEI # 1825034 Biomet, Inc. |
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