K241282
- 510(k) number
- K241282
- Device name
- RibFix Titan Fixation System
- Applicant
- Riverpoint Medical OR · US
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-08-19
- Date received
- 2024-05-07
- 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: K241282.pdf
Official FDA record: K241282
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.