Class Class II
Geister K-Rex rongeurs (K242759)
Description
Geister K-Rex rongeurs by Geister Medizin Technik GmbH, an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242759
Clearance Date2025-06-06
Clearance TypeTraditional
Product CodeHAE
Regulation Number882.4840
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242759
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Geister K-Rex rongeurs (K242759) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K223596 | SQ.line KERRISON | Aesculap, Inc. | 2023 |
| K153243 | Fehling-Punches | Fehling Instruments GmbH & Co. KG | 2016 |
Trace the full predicate network for K242759
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.