Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K092420 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Rev E PedFuse Return Screw Inserter, Part Number: 11-80030 Screw inserters are instruments which... | 2 | 08/08/2013 | SpineFrontier, Inc. |
| KRD1 PedFuse Rods, Model: IM80100-13 Rev B Product Usage: Pedicle rods are cylindrical rods whi... | 2 | 07/16/2013 | SpineFrontier, Inc. |
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