K260718
- 510(k) number
- K260718
- Device name
- mGRIP Partial Prosthesis (0.75 mm) (58669);mGRIP Partial Prosthesis (1.00 mm) (58671);mGRIP Partial Prosthesis (1.25 mm) (58673);mGRIP Partial Prosthesis (1.50 mm) (58675);mGRIP Partial Prosthesis (1.75 mm) (58677);mGRIP Partial Prosthesis (2.00 mm) (58679);mGRIP Partial Prosthesis (2.25 mm) (58681);mGRIP Partial Prosthesis (2.50 mm) (58683);mGRIP Partial Prosthesis (3.00 mm) (58685);mGRIP Partial Prosthesis (3.50 mm) (58687);mDISC Partial Prosthesis (58850)
- Applicant
- MED-EL Elektromedizinische Geräte GmbH AT
- Product code
- ETB — Prosthesis, Partial Ossicular Replacement
- Decision date
- 2026-04-03
- Date received
- 2026-03-05
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Ear, Nose, Throat
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K260718.pdf
Official FDA record: K260718
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.