K233436
- 510(k) number
- K233436
- Device name
- IlluminOss Photodynamic Bone Stabilization System
- Applicant
- Illuminoss Medical, Inc. RI · US
- Product code
- QAD — Rod, Fixation, Intramedullary And Accessories, In-Vi
- Decision date
- 2024-01-19
- Date received
- 2023-10-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K233436.pdf
Official FDA record: K233436
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.