K250494
- 510(k) number
- K250494
- Device name
- The OsteoCentric Bone Plate and Screw System
- Applicant
- OsteoCentric Technologies UT · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2025-03-18
- Date received
- 2025-02-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K250494.pdf
Official FDA record: K250494
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.