K232105
- 510(k) number
- K232105
- Device name
- APTUS Foot System 2.8-3.5
- Applicant
- Medartis AG CH
- Product code
- HRS — Plate, Fixation, Bone
- Decision date
- 2024-04-19
- Date received
- 2023-07-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K232105.pdf
Official FDA record: K232105
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.