# K001340: Stackable Cage System

- Pathway: 510(k) (Traditional)
- Applicant: Depuyacromed
- Decided: Jul 26, 2000 after 90 days
- Product code: MQP (Spinal Vertebral Body Replacement Device)
- Device class: 2
- Regulation: 21 CFR 888.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2,423 later devices descend from it; 17 cite it directly.
2 of 2,424 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021791: Verte-Stack Spinal System (2002), 2,047 descendants of its own
- K022793: Tetris Spinal Implant (2003), 1,705 descendants of its own
- K031757: Peek Tetris Spinal Implant (2003), 1,702 descendants of its own
- K020887: Ebi Ais Spine System (2002), 1,622 descendants of its own
- K040482: Ebi Esl Spine Spacer System (2004), 1,621 descendants of its own

Source page: https://510kreport.com/device/K001340
Methodology: https://510kreport.com/methodology