Contor Table Surface
Hill-Rom
FDA Clearance Information
The Contor Table Surface was cleared through the FDA 510(k) pathway on August 7, 1998. Manufactured by Hill-Rom, it is classified as a Class 2 device under product code DWJ.
What It Is
FDA-Cleared Indications
- Use as a patient-support surface during tumor ablation procedures.
- Use when stable and adjustable patient positioning is required for tumor ablation.
Clinical Applications
- Patient positioning during image-guided ablation of solid tumors.
- Support and immobilization during interventional oncology procedures involving tumor ablation.
- Patient positioning during surgical oncology procedures that require tumor ablation.
Practical Considerations
- The available FDA record identifies the device as a table surface; it does not provide enough information to confirm specific dimensions, weight limits, or adjustment ranges.
- Compatibility with CT, MRI, or other imaging systems should be confirmed in the current manufacturer documentation and with the facility's equipment before use.
- Healthcare professionals should verify patient size, positioning, weight capacity, and secure immobilization before the procedure.
- MRI safety status should not be assumed from the FDA 510(k) clearance; confirm MR Safe, MR Conditional, or MR Unsafe labeling for the specific model and configuration.
- Use should follow the manufacturer's instructions, including cleaning, inspection, and maintenance requirements.
Frequently Asked Questions
What is the Contor Table Surface used for?
The Contor Table Surface is used to provide a stable platform for tumor ablation procedures, ensuring precise patient positioning.
What specialties typically use this device?
Interventional radiologists and surgical oncologists commonly use this device during tumor ablation procedures.
What are the FDA-cleared indications?
The device is indicated for use in procedures requiring tumor ablation, particularly where precise patient positioning is necessary.