# K240690: STRUXXURE® MCS Anterior Cervical Plate System

- Pathway: 510(k) (Special)
- Applicant: Nexxt Spine
- Decided: Mar 22, 2024 after 9 days
- Product code: KWQ (Appliance, Fixation, Spinal Intervertebral Body)
- 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
Longest line of descent: 6 generations back to K953730 (1995). 23 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133475: Struxxure Anterior Cervical Plate and Screws, Nexxt Spine, LLC (2013) Summary page 4.

## Most influential descendants
- K252611: aprevo® cervical plating system (2025), 3 descendants of its own
- K260570: corra™ cervical plating system (2026), 1 descendant of its own
- K262149: corra® cervical plating system (2026), 0 descendants of its own
- K260385: aprevo® anterior and lateral lumbar interbody system; aprevo® posterior and transforaminal lumbar interbody system; aprevo® cervical interbody system; corra™ cervical plating system (2026), 0 descendants of its own

## Indications for use
The Struxxure® System is intended for anterior screw fixation of the cervical spine. These implants have been designed to provide stabilization as an adjunct to cervical fusion. Indications for the use of this implant system include degenerative disc disease (defined as neck pain of discogenic origin with the degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, trauma (i.e., fractures or dislocations), spinal stenosis, deformity (i.e., kyphosis, lordosis or scoliosis), tumor, pseudarthrosis or failed previous fusion.

Source page: https://510kreport.com/device/K240690
Methodology: https://510kreport.com/methodology