Medical Device Recalls
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31 to 31 of 31 Results
510(K) Number: K951258 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Snap Shunt Ventricular Catheter, Standard, with BioGlide, 6 CM, Ref 27708C. Each catheter is provide... | 1 | 03/27/2009 | Medtronic Neurosurgery |
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