K260934
- 510(k) number
- K260934
- Device name
- TITAN Nail; APTUS K-Wire System
- Applicant
- Medartis AG CH
- Product code
- HWC — Screw, Fixation, Bone
- Decision date
- 2026-04-17
- Date received
- 2026-03-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K260934.pdf
Official FDA record: K260934
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.