# K252546: VantageTM Lumbar Decompression Kit

- Pathway: 510(k) (Traditional)
- Applicant: Allevion Medical, LLC
- Decided: Mar 12, 2026 after 212 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K922881 (1992). 43 ancestors in all.
No later device cites it as a predicate yet.
0 of 44 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K243774: ELID (Endoscopic Less Invasive Decompression) System, Lesspine Innovations (2025). Cleared while this submission was under review Summary page 5.

## Indications for use
The Vantage™ Lumbar Decompression Kit by Allevion Medical is a specialized set of surgical instruments intended to be used to perform lumbar decompression procedures used in the treatment of various spinal conditions.

Source page: https://510kreport.com/device/K252546
Methodology: https://510kreport.com/methodology