Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K070106 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Spine & Trauma 3D Navigation 1.0 (subpart of the system Navigation Software Spine & Trauma 3D, Vers... | 1 | 04/15/2019 | Brainlab AG |
Brainlab Navigation System Spine & Trauma 3D with component Brainlab DrapeLink Registration Kit for ... | 2 | 01/05/2018 | Brainlab AG |
BrainLAB Image Guided Surgery (IGS) System, Stereotaxic Instrument navigation software, Cranial ENT... | 2 | 11/17/2015 | Brainlab AG |
Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is intended as an intraoperative image-guided l... | 2 | 08/13/2014 | Brainlab AG |
Brainlab, Spine & Trauma 3D 2.0, Navigation Software. An intraoperative image-guided localization s... | 2 | 04/17/2014 | Brainlab AG |
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