K234062
- 510(k) number
- K234062
- Device name
- APTUS Hand Scaphoid Plates
- Applicant
- Medartis AG CH
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-03-21
- Date received
- 2023-12-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K234062.pdf
Official FDA record: K234062
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.