K241269
- 510(k) number
- K241269
- Device name
- mXACT Total Prosthesis Offcenter, mXACT Total Prosthesis Center and mXACT PRO Total Prosthesis Kit
- Applicant
- MED-EL Elektromedizinische Geräte GmbH AT
- Product code
- ETA — Replacement, Ossicular Prosthesis, Total
- Decision date
- 2025-01-17
- Date received
- 2024-04-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 2.1 MB · U.S. public domain
Also available from FDA: K241269.pdf
Official FDA record: K241269
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.