Class Class II
ELID (Endoscopic Less Invasive Decompression) System (K243774)
Description
ELID (Endoscopic Less Invasive Decompression) System by Lesspine Innovations, an FDA 510(k) cleared orthopedic device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243774
Clearance Date2025-08-27
Clearance TypeTraditional
Product CodeHRX
Regulation Number888.1100
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243774
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. ELID (Endoscopic Less Invasive Decompression) System (K243774) cites 3 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K233800 | Vertos mild Device Kit (MDK-0002) | Vertos Medical, Inc. | 2024 |
| K210741 | KLS Martin Neuro Rongeurs | KLS-Martin L.P. | 2022 |
| K152734 | Kerrison Rongeurs | Vitalitec Medizintechnik GmbH | 2016 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K252546 | VantageTM Lumbar Decompression Kit | Allevion Medical, LLC | 2026 |
Trace the full predicate network for K243774
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.