K242759
- 510(k) number
- K242759
- Device name
- Geister K-Rex rongeurs
- Applicant
- Geister Medizin Technik GmbH DE
- Product code
- HAE — Rongeur, Manual
- Decision date
- 2025-06-06
- Date received
- 2024-09-12
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K242759.pdf
Official FDA record: K242759
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.