# K132328: CD Horizon Spinal System

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Sofamor Danek USA, Inc.
- Decided: Dec 6, 2013 after 133 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: 12 generations back to K040583 (2004). 74 ancestors in all.
176 later devices descend from it; 9 cite it directly.
0 of 251 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090390: CD Horizon Spinal System, Medtronic Sofamor Danek (2009) Summary page 3.
- K050439: CD Horizon Spinal System, Medtronic Sofamor Danek, Inc. (2005) Summary page 3.
- K091974: Modification to CD Horizon Spinal System, Medtronic Sofamor Danek USA, Inc. (2009) Summary page 3.
- K113174: CD Horizon Spinal System, Medtronic Sofamor Danek USA, Inc. (2011) Summary page 3.
- K981676: CD Horizon Spinal System, Sofamor Danek USA,Inc. (1999) Summary page 3.
- K101074: Modification to: CD Horizon (R) Spinal System, Medtronic Sofamor Danek USA, Inc. (2010) Summary page 3.

## Most influential descendants
- K140276: CD Horizon Spinal System (2014), 85 descendants of its own
- K142381: Xia 3 Spinal System (2014), 83 descendants of its own
- K182119: CD HORIZON™ Spinal System (2018), 58 descendants of its own
- K182928: CD Horizon™ Spinal System (2019), 53 descendants of its own
- K193011: CD Horizon™ Fenestrated Screw Set (2020), 41 descendants of its own

## Indications for use
The CD HORIZON® Spinal System with or without SEXTANT® instrumentation is intended for posterior, non-cervical fixation as an adjunct to fusion for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e., fracture or dislocation); spinal stenosis; curvatures (i.e., Icyphosis and/or lordosis); tumor; pseudarthrosis; and/or failed previous fusion. Except for hooks, when used as an anterolateral thoracic/lumbar system, the CD HORIZON® Spinal System may also be used for the same indications as an adjunct to fusion. With the exception of degenerative disc disease, the CD HORIZON® LEGACY~m 3.5mm rods and the CD HORIZONS Spinal System PEEK rods and associated components may be used for the aforementioned indications in skeletally mature patients as an adjunct to fusion. The 3.5mm rods may be used for the specific pediatric indications noted below. When used for posterior non-cervical pedicle screw fixation in pediatric patients, the CD HORIZON® Spinal System implants are indicated as an adjunct to fusion to treat adolescent idiopathic scoliosis. Additionally, the CD HORIZON® Spinal System is intended to treat pediatric patients diagnosed with the following conditions: spondylolisthesis/spondylolysis and fracture caused by tumor and/or trauma. These devices are to be used with autografi and/or allografi. Pediatric pedicle screw fixation is limited to aposterior approach. The CD HORIZON® 5PIRETm Plate isa posterior, single level, non-pedicle supplemental fixation device intended for use in the non-cervical spine (TI-SI1) as an adjunct to fision in skeletally mature patients. It is intended for plate fixation/attachment to spinous processes for the purpose of achieving supplemental fixation in the following conditions: degenerative disc disease (as previously defined); spondylolisthesis; trauma; and/or tumor. In order to achieve additional levels of fixation, the CD HORIZON® Spinal System rods may be connected to the VERTEX® Reconstruction System with the VERTEX® rod connector. Refer to the VERTEX®D Reconstruction System Package Insert for a list of the VERTEX® indications of use.

Source page: https://510kreport.com/device/K132328
Methodology: https://510kreport.com/methodology