K253300
- 510(k) number
- K253300
- Device name
- Fine Osteotomy
- Applicant
- Bodycad Laboratories, Inc. CA
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2025-10-28
- Date received
- 2025-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253300.pdf
Official FDA record: K253300
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.