# K253990: KHEIRON® Spinal Fixation System, including patient specific K-ROD

- Pathway: 510(k) (Special)
- Applicant: S.M.A.I.O
- Decided: Jan 7, 2026 after 26 days
- Product code: NKB (Thoracolumbosacral Pedicle Screw System)
- Device class: 2
- Regulation: 21 CFR 888.3070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 26 generations back to K040583 (2004). 510 ancestors in all.
2 later devices descend from it; 2 cite it directly.
1 of 513 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211981: KHEIRON® Spinal Fixation System, S.M.A.I.O (2022) Summary page 5.
- K232650: KHEIRON® Spinal Fixation System, including patient specific K-ROD, S.M.A.I.O (2023) Summary page 5.
- K251804: KHEIRON® Spinal Fixation System, including patient specific K-ROD, S.M.A.I.O (2025) Summary page 5.
- K200245: EXPEDIUM® Spine System; EXPEDIUM VERSE® Spine System, Medos International Sàrl (2020) Summary page 5.
- K231479: TriALTIS Spine System, Medos International SARL (2023) Summary page 5.

## Most influential descendants
- K260786: KHEIRON® Spinal Fixation System, including patient specific K-ROD (2026), 1 descendant of its own
- K262828: KHEIRON® Spinal Fixation System, including patient specific K-ROD (2026), 0 descendants of its own

## Indications for use
KHEIRON@ Spinal Fixation System including patient specific K-ROD is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of thoracic, lumbar, and sacral spine: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, deformities or curvatures (i.e. scoliosis, kyphosis, and/or lordosis), spinal stenosis, spinal tumor, pseudarthrosis and failed previous fusion. When used for posterior, non-cervical, pedicle screw fixation in pediatric patients, KHEIRON® Spinal Fixation System including patient specific K-ROD is indicated as an adjunct to fusion to treat progressive spinal deformities (i.e., scoliosis, kyphosis, or lordosis) including idiopathic scoliosis, neuromuscular scoliosis, and congenital scoliosis. Additionally, KHEIRON@ Spinal Fixation System including patient specific K-ROD is intended to treat pediatric patients diagnosed with spondylolisthesis/spondylolysis, fracture caused by tumor and/or trauma, pseudarthrosis, and/or failed previous fusion. This system is intended to be used with autograft and/or allograft. Pediatric pedicle screw fixation is limited to a posterior approach. Patient specific K-ROD devices are compatible with NuVasive Reline System components and Seaspine Mariner System components that are compatible with 05.5 mm and/or o6.0 mm rods as well as screws 04.5mm or larger and at least 25 mm in length. Patient specific K-ROD devices are compatible with Seaspine Mariner System components that are compatible with o5.5 mm and/or o6.0 mm rods as well as screws o4.5 mm or larger and at least 25 mm in length. Patient specific K-ROD devices are compatible with VitalTM Spinal Fixation System components that are compatible with o5.5mm and/or o6.Omm rods as well as screws o4.Omm or larger and at least 20mm in length. Patient specific K-ROD devices are compatible with Depuy Expedium@ and TriALTIST r Spine Systems components that are compatible with o5.5mm and/or o6.0 mm rods as well as screws o4.35m or larger for Expedium@ Spine System and fenestrated screws o4.50 mm or larger for TriALTIST-r Spine system.

Source page: https://510kreport.com/device/K253990
Methodology: https://510kreport.com/methodology