K250711
- 510(k) number
- K250711
- Device name
- VSP Orthopedics System
- Applicant
- 3D Systems, Inc. CO · US
- Product code
- PBF — Orthopaedic Surgical Planning And Instrument Guides
- Decision date
- 2025-12-05
- Date received
- 2025-03-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K250711.pdf
Official FDA record: K250711
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.