K251709
- 510(k) number
- K251709
- Device name
- MedCAD® AccuStride System
- Applicant
- Medcad TX · US
- Product code
- PBF — Orthopaedic Surgical Planning And Instrument Guides
- Decision date
- 2025-11-04
- Date received
- 2025-06-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251709.pdf
Official FDA record: K251709
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.