Important Safety Information

Spine Endoscopes and Accessories

Indications

The Arthrex spine endoscope is a medical device that helps doctors view and access spinal structures during ultra-minimally invasive procedures. It is used to give the surgeon a clear view while performing endoscopic spine surgery.

Contraindications

This device should not be used if your doctor determines that endoscopic spine surgery is not safe or appropriate for your condition. It also should not be used if the surgical environment does not meet the necessary safety and equipment standards required for this type of procedure.

Warnings

This device is used only by trained medical professionals, and your surgeon will decide whether it is appropriate for your specific condition. Your surgical team follows strict safety procedures, including checking all instruments before surgery, using only sterile and single use items as intended, and disposing of medical waste safely. They also monitor the equipment throughout the procedure to ensure clear visibility and proper function, and they take steps to prevent issues such as fogging, debris buildup, or heat from surgical tools. Your surgeon will avoid using the endoscope near MRI machines or certain types of imaging equipment when it could pose a risk. If any equipment concerns or unexpected issues arise, your surgical team will address them immediately to help ensure your safety.

If you have any questions or concerns, please discuss them with your healthcare provider.

Spine Compression FT Screws 

Indications 

Arthrex Spine Compression FT Screws are implantable devices used to help stabilize and support healing in certain conditions affecting the cervical (neck), thoracic (mid-back), and lumbar (lower back) spine. They may be used as part of a spinal fusion procedure or to repair specific spinal fractures or defects, including pars fractures, for the adolescent and adult population (12-21 years of age). 

Contraindications 

These implants may not be appropriate for all patients. They should not be used in patients with active infection, inadequate bone quality or quantity, certain medical conditions that may interfere with healing, or other situations where the surgeon determines the device is not suitable. Your doctor will evaluate your condition and medical history to determine whether this treatment option is right for you. 

Warnings 

These implants are intended for use only by trained medical professionals. As with any spine surgery, there are potential risks, including infection, implant loosening or breakage, nerve injury, failure of the bone to heal properly, and the possible need for additional surgery. Successful healing depends on many factors, including bone quality, the nature of the condition being treated, and following your surgeon's postoperative instructions. Patients may be asked to limit certain activities during recovery to help protect the repair while healing occurs. 

These implants are designed for single-patient use only and must not be reused. The implants are MR Conditional, which means patients may be able to undergo MRI examinations under specific conditions. Be sure to inform all healthcare providers that you have a spinal implant before any imaging procedure. 

If you have any questions or concerns, please discuss them with your healthcare provider. 

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