K232693
- 510(k) number
- K232693
- Device name
- Tyber Medical Distal Radius Plating System
- Applicant
- Tyber Medical, LLC PA · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2023-12-04
- Date received
- 2023-09-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K232693.pdf
Official FDA record: K232693
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.