Status: Recruiting
FIBERGRAFT Aeridyan Posterolateral Fusion Study
This is a post-market, prospective, controlled, multicenter clinical study to evaluate radiographic fusion and clinical outcomes of FIBERGRAFT™ Aeridyan Matrix bone graft substitute in subjects who undergo a 1-3 level instrumented lumbar posterolateral fusion surgery. This clinical study will be conducted at up to 10 clinical sites within the United States.
Participants needed: 316
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: DePuy Synthes Products, Inc.Updated: Jun 5, 2026Locations: 8
Eligibility criteria
Subjects who require a 1-3 level instrumented PLF fusion in the lumbar spine in... [+2]
Subjects who had previous fusion surgery at the index level(s). [+17]