K250923
- 510(k) number
- K250923
- Device name
- Fine Osteotomy
- Applicant
- Bodycad Laboratories, Inc. CA
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2025-08-21
- Date received
- 2025-03-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K250923.pdf
Official FDA record: K250923
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.