# K111354: GS Medical Anyplus Peek Lumbar Cages (Alif and Dlif)

- Pathway: 510(k) (Special)
- Applicant: GS Medical Co., Ltd.
- Decided: Oct 17, 2011 after 157 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: 2 generations back to P960025 (1999). 3 ancestors in all.
11 later devices descend from it; 3 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100516: Anyplus Peek Cages, GS Medical Co., Ltd. (2010) Summary page 1.

## Most influential descendants
- K131612: Anyplus; Alif Peek Cages, Plif Peek Cages, T-Plif Peek Cages, Tlif Peek Cages (2014), 8 descendants of its own
- K243074: Spectrum Spine Lumbar Cage System (2025), 2 descendants of its own
- K221719: ABTross ALIF Expandable Cage System (2022), 2 descendants of its own
- K212980: Tesera-k ALIF System (2022), 2 descendants of its own
- K242771: Tesera-k PL System and Tesera-k XL System (2025), 1 descendant of its own

## Indications for use
AnyPlus® PEEK Lumbar Fusion Cage device is intended for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s).

Source page: https://510kreport.com/device/K111354
Methodology: https://510kreport.com/methodology