ChoiceSpine Granted FDA Clearance of Triton SI Joint System

By Julie A. Vetalice

ChoiceSpine Granted FDA Clearance of Triton SI Joint System

ChoiceSpine received FDA 510(k) clearance to market the Triton Sacroiliac Joint Fixation System.

Triton SI Joint fixation is a 3D-printed screw intended for sacroiliac joint fixation for conditions including degenerative sacroiliitis and sacroiliac joint disruption. The system features ChoiceSpine’s propriety BioBond™, porous structure technology. The cannulated screw allows for in situ graft delivery with open and porous graft windows designed to promote bone growth. Triton offers three screw diameters: 8mm secondary, 12mm primary, and 14mm revision with lengths 30-65mm in 5mm increments.

The Triton SI Joint Fixation System includes:

  • Open and porous graft openings for continuous porosity
  • Cannulated screws to allow for in-situ graft delivery to promote bone growth
  • Secure driver interface and internal threads for driver retention
  • Simple and easy-to-use instrumentation designed to reduce surgical steps in the operating room
  • Sterilized 3D-printed screws to maximize patient safety

Source: ChoiceSpine LLC

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory