K261898
- 510(k) number
- K261898
- Device name
- Triathlon® Knee System; Triathlon® Hinge Knee System; Scorpio® Total Knee System
- Applicant
- Howmedica Osteonics Corp. dba Stryker Orthopaedics NJ · US
- Product code
- KRO — Prosthesis, Knee, Femorotibial, Constrained, Cemente
- Decision date
- 2026-08-06
- Date received
- 2026-06-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K261898.pdf
Official FDA record: K261898
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.