The OsteoCool™ RF ablation probe kit, in combination with other components of the OsteoCool™ RF ablation system, is intended for palliative treatment in spinal procedures by ablation of metastatic malignant lesions in a vertebral body.
Use of the OsteoCool™ RF ablation system device is contraindicated in vertebral body levels C1–C7.
Introducers must be 13 Gauge or larger, and have a length such that the proximal electrode on the probe is extended at least 5 mm beyond the distal margin of the introducer.
The OsteoCool™ RF ablation probe kit is used with other components of the OsteoCool™ RF ablation system in RF lesion procedures. Adverse events associated with the use of this device are similar to those indicated for medicated and anesthetic methods used in other surgical procedures.
Candidates suitable for RF ablation procedures with the OsteoCool™ RF ablation system include:
Patients should be examined prior to the RF ablation procedure to determine the focal site(s) of pain. The following should be used to help guide therapy and define the area that is intended for RF ablation:
Per the indications for use, the device is intended for:
Standard therapy is defined per relevant medical society guidelines on treatment of metastatic lesions involving bone. For guidance, please refer to applicable medical society guidelines.
The OsteoCool™ RF ablation bone access kits are indicated for percutaneous access to bone.
Find more information, including other available configurations, for OsteoCool™ RF ablation system.
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