K261032
- 510(k) number
- K261032
- Device name
- NovoKnee (SteriKnee)
- Applicant
- NovoSource WV · US
- Product code
- JWH — Prosthesis, Knee, Patellofemorotibial, Semi-Constrai
- Decision date
- 2026-04-27
- Date received
- 2026-03-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K261032.pdf
Official FDA record: K261032
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.