K242896
- 510(k) number
- K242896
- Device name
- Caliber Intramedullary Fixation System
- Applicant
- Nvision Biomedical Technologies TX · US
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2025-02-05
- Date received
- 2024-09-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K242896.pdf
Official FDA record: K242896
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.