K261651
- 510(k) number
- K261651
- Device name
- Precice Max System and Precice Ankle Salvage System
- Applicant
- NuVasive Specialized Orthopedics PA · US
- Product code
- HSB — Rod, Fixation, Intramedullary And Accessories
- Decision date
- 2026-06-18
- Date received
- 2026-05-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K261651.pdf
Official FDA record: K261651
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.