Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K993021 |
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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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| Medtronic Sofamor Danek brand METRx System 16 mm Med Procedure Kit; Ref 9560016. | 2 | 07/13/2005 |
FEI # 1824199 Warsaw Orthopedic, Inc. |
| Medtronic Sofamor Danek brand METRx System MD Procedure Kit; Ref 9560030. | 2 | 07/13/2005 |
FEI # 1824199 Warsaw Orthopedic, Inc. |
| Medtronic Sofamor Danek brand METRx System 18 mm Med Procedure Kit; Ref 9560018. | 2 | 07/13/2005 |
FEI # 1824199 Warsaw Orthopedic, Inc. |
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