# K190364: CancelleX Porous Titanium Lumbar Interbody Device

- Pathway: 510(k) (Traditional)
- Applicant: Xenco Medical, LLC
- Decided: Apr 18, 2019 after 62 days
- Product code: MAX (Intervertebral Fusion Device With Bone Graft, Lumbar)
- Device class: 2
- Regulation: 21 CFR 888.3080
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K230219: Eminent Spine 3D Lumbar Interbody Fusion Systems (2023), 4 descendants of its own
- K243074: Spectrum Spine Lumbar Cage System (2025), 2 descendants of its own
- K253260: ORIO-3D Cage System (2026), 0 descendants of its own
- K252240: Spectrum Spine Cervical Cage System; Spectrum Spine Lumbar Cage System (2026), 0 descendants of its own
- K253377: Expandable Titanium PLIF/TLIF System (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K190364
Methodology: https://510kreport.com/methodology