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Recall Observatory FDA recall evidence

Device product

Navigation Spine & Trauma 3D Version 2.0 and 2.1 Is intended as an intraoperative image-guided localization system to enable minimally invasive surgery. It links a freehand probe, tracked by a passive marker sensor system to virtual computer image space on a patient's preoperative or Intraoperative 2D or 3D image data. The system is indicated for any medical condition in which the use of stereotactic surgery may be appropriate and where a reference to a rigid anatomical structure, such as the skull, the pelvis, a long bone or vertebra can be identified relative to the acquired image (CT, MR, 2D fluoroscopic image or 3D fluoroscopic image reconstruction) and/or an image data based model of the anatomy.

Z-2213-2014

May 21, 2014

Class II

Product summary

Firm
Brainlab AG
Event
Event 68845
Status
Terminated
Classification
Class II
Quantity
17 systems
Official record key
device-enforcement:Z-2213-2014

Official wording

Reason: Brainlab Navigation Software Spine & Trauma 3D 2.0/2.1 offers automatic registration of intraoperatively acquired CT image data sets. To enable automatic registration, the software requires the gantry position of the scanner. The gantry position can either be entered manually or submitted automatically from the CT scanner. If automatic gantry communication is available, the so-called &quot

Code information: Model/Catalog Number: 19061-03

Distribution pattern: Worldwide distribution: US (nationwide) including states of: NC, NY, OH, WI;and countries of: Austria, China, Germany, Italy, Japan, Malaysia, and Saudi Arabia.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software requires the gantry position of the scanner. The gantry position can