Medical Device Recalls
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1 result found
510(K) Number: K010322 |
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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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Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic Distractor. The ISKD is ... | 2 | 02/28/2013 | Orthofix, Inc |
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