# K223627: PreView-III™ Anterior Cervical Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Nexus Spine, LLC
- Decided: Feb 2, 2023 after 59 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: 1 generation back to K062371 (2006). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K062371: Preview Anterior Cervical Plate System, Alphaspine, Inc. (2006) Summary page 4.

## Most influential descendants
- K261279: DeltaNEC Interbody System (2026), 0 descendants of its own

## Indications for use
The PreView-11I™ Anterior Cervical Plate System is intended for the treatment of the cervical spine in skeletally mature patients receiving fusion by autogenous and/or allogenic bone graft. The implants are attached to the anterior cervical spine (C2-T1). PreView-I1I™ Anterior Cervical Plate System is intended for use under the following indications degenerative disc disease (defined as neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), spondylolisthesis, trauma (i.e., fracture), tumor, deformity (i.e., kyphosis, lordosis, and scoliosis), spinal stenosis, pseudoarthrosis, and failed previous fusion.

Source page: https://510kreport.com/device/K223627
Methodology: https://510kreport.com/methodology