Device Recall TiBond

  • Modèle / numéro de série
    All revisions
  • Classification du dispositif
  • Classe de dispositif
  • Dispositif implanté ?
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 || This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months non-operative treatment prior to being treated with this device.
  • Manufacturer
  • 1 Event


  • Adresse du fabricant
    Spinal Elements, Inc, 3115 Melrose Dr, Suite 200, Carlsbad CA 92010-6690
  • Source