Medical Device Recalls
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1 result found
510(K) Number: K092624 |
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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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Ratcheting Torque Limiting Handle, Catalog Number 52-1012, Orthofix Spinal Implants, Firebird Spinal... | 2 | 09/07/2011 | Orthofix, Inc. |
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