Medical Device Recalls
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1 result found
510(K) Number: K033669 |
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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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PERI-LOC (R), 3.5 MM ANTEROLATERAL DISTAL TIBIA PLATE, 10 HOLE, RIGHT - 148 MM, REF 71800710, QTY: ... | 2 | 08/31/2010 | Smith & Nephew Inc |
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