U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel data.
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Package insert incorrect.
조치
Spine Wave notified each affected customer on October 22,2010, via telephone of the product, the issue and action they should take. Customers were asked to segregate the product from other products and immediately return to Spine Wave.
For questions regarding this recall call 203-944-9494.
Nationwide Distribution including Delaware, Massachusetts, Maryland, and New York
제품 설명
StaXx¿ XD Expandable Cartridge Convex Expandable Implant 25mm (L) x 9mm (W) x 7mm (H) || Catalog number: 11-1525 || The StaXx¿ XD System is a vertebral body replacement device intended for use in the thoracolumbar spine (TI-L5) to replace and restore height of a collapsed, damaged, or unstable vertebral body or portion thereof, due to tumor or trauma (i.e., fracture). The system is to be placed bilaterally and used with autograft or allograft and supplemental spinal fixation. The supplemental fixation system that is intended to be used with the StaXx¿ XD System is the CapSure¿ PS Spine System.