Medical Device Recalls
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1 result found
510(K) Number: K012366 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Nexframe® Stereotactic System Kits, Model Number(s): DB-1021-MR, DB-1031, DB-1040-BL, DB-1040-ST, DB... | 2 | 02/07/2008 |
FEI # 3002684500 Medtronic Image Guided Neurologics, Inc. |
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