# K091926: Choice Spine Anterior Cervical Plate (Acp) System

- Pathway: 510(k) (Traditional)
- Applicant: Choicespine, LP
- Decided: Dec 22, 2009 after 175 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
No predicates in its family tree.
2 later devices descend 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)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K173867: Axis Anterior Cervical Plate System (2018), 1 descendant of its own
- K203154: KASILOF Cervical Plate System (2020), 0 descendants of its own

## Indications for use
The Choice Spine Anterior Cervical Plate (ACP) System is intended for anterior screw fixation of the cervical spine (levels C2 to C7) and is designed to provide stabilization as an adjunct to spinal fusion at these levels. Indications for the use of this device include: failed previous fusion, pseudoarthrosis, tumor, deformity, spinal sternosis, trauma, spondylolisthesis, or degenerative disc disease defined as neck pain of disdogenic origin with the degeneration of the disc confirmed by history and radiographic studies. WARNING: The Choice Spine Anterior Cervical Plate ('ACP) System is not intended for screw attachment or fixation to the posterior elements (pedicles) of the cervical, thoracic or lumbar spine.

Source page: https://510kreport.com/device/K091926
Methodology: https://510kreport.com/methodology