K232176
- 510(k) number
- K232176
- Device name
- STELLAR Knee
- Applicant
- Polarisar, Inc. FL · US
- Product code
- SBF — Orthopedic Augmented Reality
- Decision date
- 2023-11-02
- Date received
- 2023-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K232176.pdf
Official FDA record: K232176
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.