ELEOS¿ LIMB SALVAGE SYSTEM
Received May 20, 2026 · Event occurred Apr 22, 2026
Report 3013450937-2026-00206 · MDR key 25229614
Device
Generic name
Eleos¿ Tibial Poly Spacer 8mm
Manufacturer
Onkos Surgical Inc.Catalog number
25001208E
Lot number
2024443
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
16 YR · Female
- Medical device site infection
Narrative
Additional Manufacturer Narrative
THE ROOT CAUSE OF THIS COMPLAINT WAS NOT DETERMINED. BASED ON THE REVIEW OF KNOWN DEVICE HISTORY RECORDS, THE INVESTIGATION CONCLUDED THAT THE ROOT CAUSE OF THE ALLEGED INFECTION WAS NOT RELATED TO THE DESIGN, MANUFACTURE, AND/OR STERILIZATION OF THE REVISED IMPLANTS.
Description of Event or Problem
IT WAS REPORTED BY AN ONKOS SALES REPRESENTATIVE, THAT A PATIENT WITH AN ELEOS DISTAL FEMUR REPLACEMENT UNDERWENT REVISION SURGERY ON (B)(6) 2026 DUE TO AN ALLEGED INFECTION. THIS REPORT CAPTURES ELEOS POLY SPACER. THIS EVENT WILL BE REPORTED AS A SERIOUS INJURY DUE TO THE REVISION PROCEDURE.