# K081132: Spinesmith Partners, LP Cequence Anterior Cervical Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Spine Smith Partners L.P.
- Decided: Jul 14, 2008 after 84 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.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The SpineSmith Cequence Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine at one level between C2-C7 for the following indications: · Degenerative disc disease [DDD] - defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies * Spondylolisthesis · Spinal Stenosis · Tumors · Trauma (i.e. fracture)

Source page: https://510kreport.com/device/K081132
Methodology: https://510kreport.com/methodology