Medical Device Recalls
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1 result found
510(K) Number: K053159 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BrainLAB's VectorVision spine is intended for use as an intraoperative image-guided localization sys... | 2 | 02/10/2014 | Brainlab AG |
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