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# Sail Fusion Sacroiliac Fusion Device Cleared
- URL: https://www.fdaweb.com/sail-fusion-sacroiliac-fusion-device-cleared/
- Published: 2024-04-23T12:00:00.000Z
- Updated: 2026-09-14T14:28:57.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156834

FDA has cleared a Sail Fusion 510(k) for its BowTie Sacroiliac Fusion System. The device features a novel bowtie shape as well as integrated transfixation and iliac screws to maximize rigidity, the company says. “It also utilizes a proprietary porous structure and roughened surface technology to facilitate osteointegration,” it adds. Additionally, the BowTie rigidly fixates the joint to provide a biologic environment favorable for bone growth. “We reinforced its rigidity by adding both integrated iliac and transfixation screws to address the complex biomechanics of the pelvis,” Sail Fusion says.