K242973
- 510(k) number
- K242973
- Device name
- CanMINI Hand and Foot System
- Applicant
- Canwell Medical Co., Ltd. CN
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2025-04-24
- Date received
- 2024-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K242973.pdf
Official FDA record: K242973
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.