# K082821: Spinesmith Partners, LP Cequence Anterior Cervical Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Spine Smith Partners L.P.
- Decided: Oct 31, 2008 after 36 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 (C2-C7) as an adjunct to fusion in the treatment of 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/K082821
Methodology: https://510kreport.com/methodology