K233696
- 510(k) number
- K233696
- Device name
- DePuy Synthes Retrograde Femoral Nail Advanced System
- Applicant
- DePuy Synthes PA · US
- Product code
- HSB — Rod, Fixation, Intramedullary And Accessories
- Decision date
- 2024-08-01
- Date received
- 2023-11-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K233696.pdf
Official FDA record: K233696
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.