Devices

Cavity SpineWand

  • Model / Serial
    Lot Numbers: 1024313, 1024482, 1027160, 1034306, 1041879, 1059328
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    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.
  • Product Description
    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

Manufacturer

ArthroCare Corporation
  • Manufacturer Address
    ArthroCare Corporation, 7000 W William Cannon Dr, Austin TX 78735-8509
  • Manufacturer Parent Company (2017)
    Smith & Nephew plc
  • Source
    USFDA

4 devices with a similar name

Learn more about the data here

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