# K050588: Verteview Anterior Cervical Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Innovative Spinal Design, LLC
- Decided: Apr 21, 2005 after 44 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 K010003 (2001). 2 ancestors in all.
16 later devices descend from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030866: Synthes Anterior CSLP System, Synthes (Usa) (2003) Summary page 1.
- K010003: Ebi Vuelock Anterior Cervical Plate System, Ebi, L.P. (2001) Summary page 1.

## Most influential descendants
- K121060: Spine Frontier Indus Acp System (2012), 15 descendants of its own
- K153526: Pyrenees Cervical Plate System (2016), 6 descendants of its own
- K140234: Aspiron Acp System (2014), 6 descendants of its own
- K162664: Pyrenees Cervical Plate System (2016), 5 descendants of its own
- K182473: PYRENEES Cervical Plate System, BLUE RIDGE Cervical Plate System, OZARK Cervical Plate System, CAYMAN Thoracolumbar and Buttress Plate Systems (2018), 4 descendants of its own

## Indications for use
This system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusions in patients with 1) degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), 2) trauma (i.e., fractures or dislocation), 3) tumors, 4) spinal stenosis, 5) spondylolisthesis, 6)deformity or curvatures (i.e., kyphosis and/or lordosis, or scoliosis), 7) pseudoarthrosis, and/or 8) failed previous fusions.

Source page: https://510kreport.com/device/K050588
Methodology: https://510kreport.com/methodology