K253906
- 510(k) number
- K253906
- Device name
- Xpert Hand
- Applicant
- Newclip Technics FR
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2026-03-11
- Date received
- 2025-12-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K253906.pdf
Official FDA record: K253906
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.