Eminent Spine's 3D Printed Titanium Posterior SI System Earns FDA Approval
Eminent Spine introduces a cutting-edge solution for patients and surgeons with its 3D Printed Titanium Posterior SI System designed to enhance SI joint fusion procedures. This innovative system is specifically engineered to compress and transfix the sacroiliac (SI) joint, reflecting a significant advancement in spinal implant technology.
Innovative Features of the SI System
The system's design caters to the needs of both surgeons and patients, incorporating advanced engineering techniques. Some of the notable features include:
- Compression and transfixation capabilities for the SI joint.
- Aggressive lordotic teeth that help minimize implant migration.
- A spacious central opening optimized for bone graft materials.
- Tapered nose and rounded edges designed for seamless insertion.
Technical Specifications
The implant dimensions are set at 25mm x 14mm x 8mm, making it an effective choice for various surgical contexts. Surgeons can choose from screw options of either 3.5 or 3.75mm in length, with a range from 10 to 18mm. Additionally, built-in locking tabs on the implants provide added security during procedures.
Commitment to Safety and Efficacy
Through rigorous biomechanical testing and validation, Eminent Spine has confirmed the efficacy of its innovative design. With FDA 510(k) clearance received, the 3D Printed Titanium Posterior SI System complies with high standards for safety and clinical outcomes. This milestone marks a notable achievement for Eminent Spine, demonstrating its commitment to advancing spinal health solutions.
The Vision Behind Eminent Spine
Eminent Spine was established to revolutionize spinal solutions by focusing on high-performance implants driven by the needs of surgeons and patients alike. Through a commitment to biomechanical excellence and enhanced recovery times, the company is at the leading edge of orthopedic innovation.
Future Implications for SI Joint Procedures
With the successful FDA clearance of this advanced system, Eminent Spine plans to further streamline procedures for treating SI joint dysfunction. According to Dr. Stephen Courtney, Founder and CEO, this FDA approval enables the offering of a well-rounded and comprehensive approach for patient care.
Contact Information
For further insights or to explore demonstrations of the 3D Printed Titanium Posterior SI System, reach out to Eminent Spine at:
Eminent Spine
Phone: 972-499-3593
Website: www.eminentspine.com
Frequently Asked Questions
What is the 3D Printed Titanium Posterior SI System?
This system is an innovative spinal implant designed to treat sacroiliac joint dysfunction by compressing and transfixing the joint.
Who developed this SI System?
Eminent Spine, an organization dedicated to spinal innovation, developed the system with a focus on patient and surgical needs.
What are the key features of this system?
Notable features include aggressive lordotic teeth for stability, a large opening for bone grafts, and an ergonomic design for easy insertion.
How does FDA approval benefit patients?
FDA clearance signifies that the system meets stringent safety and efficacy standards, ensuring reliable clinical outcomes for patients.
Where can I find more information about the system?
For detailed information and demonstrations, visit Eminent Spine's official website at www.eminentspine.com.
