Medical Device Recalls
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1 result found
510(K) Number: K991590 |
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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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| Electronic Otto Bock Compact leg prosthesis System, 3C95/3C85, to be used exclusively for the exopro... | 2 | 01/25/2007 |
FEI # 2182293 Bock,Otto,Orthopedic Ind,Inc |
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