K261054
- 510(k) number
- K261054
- Device name
- RibPlate System
- Applicant
- Stryker Leibinger GmbH & Co KG DE
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2026-07-01
- Date received
- 2026-03-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.4 MB · U.S. public domain
Also available from FDA: K261054.pdf
Official FDA record: K261054
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.