K232267
- 510(k) number
- K232267
- Device name
- Precice Max System
- Applicant
- Nuvasive Specialized Orthopedics, Incorporated CA · US
- Product code
- HSB — Rod, Fixation, Intramedullary And Accessories
- Decision date
- 2023-12-15
- Date received
- 2023-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232267.pdf
Official FDA record: K232267
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.