Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K930511 |
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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 METRx (TM) System Bayonet Electrosurgical Pencil, sterile, Manufactured at W... | 2 | 11/07/2007 |
FEI # 1824199 Warsaw Orthopedic, Inc. dba Medtronic SOFAMOR DANEK |
| Bayonet Electrosurgical Pencil. P/N 9560575. The product is shipped in cases containing 100 blades/p... | 2 | 08/14/2007 |
FEI # 1000135710 Zinnanti Surgical Design LLC |
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