Devices

Cavity SpineWand

  • Modelo / Serial
    Lot Numbers: 1024313, 1024482, 1027160, 1034306, 1041879, 1059328
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution. US nationwide including OH, MO, AZ, AL, CA, FL, SC, GA, and PA; Spain, France, United Kingdom, Germany, Switzerland, Singapore, Russia, Turkey, and Ecuador.
  • Descripción del producto
    Cavity 8 Gauge Spine Wand indicated for resection, ablation, and coagulation of soft tissues and hemostasis of blood vessels in spinal procedures.
  • Manufacturer
    ArthroCare Corporation
  • 1 Event

Fabricante

ArthroCare Corporation
  • Dirección del fabricante
    ArthroCare Corporation, 7000 W William Cannon Dr, Austin TX 78735-8509
  • Empresa matriz del fabricante (2017)
    Smith & Nephew plc
  • Source
    USFDA

4 dispositivos con un nombre similar

Más información acerca de la data acá

Coblation Electrode - Cavity Spinewand
CAVITY SpineWand Device, 8-gauge
  • Modelo / Serial
  • Descripción del producto
    CAVITY SpineWand Device, 8-gauge, ArthroCare Corporation
  • Manufacturer
    Smith & Nephew Pte Limited
Cavity SPINEWAND device, 8-gauge
  • Modelo / Serial
  • Descripción del producto
    ArthroCare Corporation: Cavity SPINEWAND device, 8-gauge
  • Manufacturer
    ArthroCare Corporation
Cavity SPINEWAND Device, 8-gauge
  • Modelo / Serial
    KP-CAV-7705-01 | 1024313, 1024482, 1027160, 1034306, 1041879, 1059328
  • Descripción del producto
    MD: Universal foot-controlled electrosurgical diathermy system conducting unit, single-use
  • Manufacturer
    ArthroCare Corporation