Medical Device Recalls
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1 result found
510(K) Number: K151488 |
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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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| Firebird Spinal Fixation System Torque Limiting Handle (PN 52-1512) Intended for posterior, non-c... | 2 | 02/11/2016 | Orthofix, Inc |
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