Illico Ti Cannulated Polyaxial Screw

  • Modelo / Serial
    Product Codes: KW, MNI, MNH.  Part NumberlLot Number: ¿PART DESCRIPTION LOT  7384S-30 Ti CANNULATED POLYAXIAL SCREW 4.5mm X 30mm 646501  73845-35 Ti CANNULATED POLYAXIAL SCREW 4.5mm X 35mm 646502  73845-40 Ti CANNULATED POLYAXIAL SCREW 4.5mm X 40mm 646503  73845-45 Ti CANNULATED POLYAXIAL SCREW 4.5mm X 45mm 646504  73855-35 Ti CANNULATED POLYAXIAL SCREW 5.5mm X 35mm 646510  73865-30 Ti CANNULATED POLYAXIAL SCREW 6.5mm X 30mm 646515  73865-35 Ti CANNULATED POLYAXIAL SCREW 6.5mm X 35mm 646516  73865-40 Ti CANNULATED POLYAXIAL SCREW 6.5mm X 40mm 646517  73865-45 Ti CANNULATED POLYAXIAL SCREW 6.5mm X 45mm 646542  73865-50 Ti CANNULATED POLYAXIAL SCREW 6.5mm X 50mm 646543  73875-35 Ti CANNULATED POLYAXIAL SCREW 7.5mm X 35mm 646546  73875-45 Ti CANNULATED POLYAXIAL SCREW 7.5mm X 45mm 646548  73875-50 Ti CANNULATED POLYAXIAL SCREW 7.5mm X 50mm 646549
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    Nationwide Distribution including AZ, IL, CA, SC, TN, TX, GA, CT, NY, FL, OK, LA, MO, NV,and UT.
  • Descripción del producto
    ILLlCO¿ MIS Posterior Fixation System, Bone-screw Internal Spinal Fixation System, || Orthosis, Spinal Pedical Fixation || Orthosis, Spondylolisthesis Spinal Fixation || The ILLICO MIS Posterior Fixation System is intended to facilitate the surgical correction of noncervical spinal deformities by providing temporary internal fixation and stabilization during bone graft healing and/or fusion mass development. When used for a minimally invasive posterior approach ILLlCO¿ MIS Instrumentation is used in conjunction with polyaxial screw components. The ILLICO MIS Posterior Fixation System is intended for use as a posterior spinal fixation device to aid in the surgical correction of various spinal deformities and pathologies of the spine. It is intended to provide stabilization during the development of fusion utilizing a bone graft. Specific indications for the ILLICO MIS Posterior Fixation System are dependent in part on the configuration of the assembled device and the method of attachment to the spine.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Alphatec Spine, Inc., 5818 El Camino Real, Carlsbad CA 92008-8816
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA