DiFusion receives FDA 510K clearance for Xiphos-ZF Spinal interbody device

Press/Media

Period6 Nov 2019

Media coverage

1

Media coverage

  • TitleDiFusion receives FDA 510K clearance for Xiphos-ZF Spinal interbody device
    Media name/outletPharmaBiz
    Country/TerritoryIndia
    Date6/11/19
    PersonsStephen Badylak