# K151020: Rampart-T Interbody Fusion System

- Pathway: 510(k) (Special)
- Applicant: Spineology, Inc.
- Decided: Jul 22, 2015 after 97 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
Longest line of descent: 6 generations back to K111880 (2011). 9 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110933: Spineology Peek Lumbar Interbody Fusion Device, Spineology, Inc. (2011) Summary page 4.
- K111880: Spineolgy Peek Bullet Lumber Interbody Fusion Device, Spineology, Inc. (2011) Summary page 4.
- K132053: Rampart-O, Rampart-T, Spineology, Inc. (2013) Summary page 4.
- K113030: Spineology Peek Bullet Lumbar Interbody Fusion Device, Spineology, Inc. (2012) Summary page 4.

## Most influential descendants
- K163409: Rampart (TM) T Lumbar Interbody Fusion Device (2017), 0 descendants of its own

## Indications for use
Rampart-T implants are intervertebral body fusion devices indicated for intervertebral body fusion at one level or two contiguous levels in the lumbar spine from L2 to S1 in patients with degenerative disc disease (DDD) with up to Grade I spondylolisthesis at the involved level(s). DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies. These patients should be skeletally mature and have had six months of non-operative treatment. Rampart-T implants are designed for use with autograft to facilitate fusion and are intended for use with supplemental fixation systems cleared by the FDA for use in the lumbar spine.

Source page: https://510kreport.com/device/K151020
Methodology: https://510kreport.com/methodology