# K173521: SeaSpine Cabo ACP (Anterior Cervical Plate) System

- Pathway: 510(k) (Traditional)
- Applicant: SeaSpine Orthopedics Corporation
- Decided: Jan 24, 2018 after 71 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: 8 generations back to K922087 (1992). 29 ancestors in all.
15 later devices descend from it; 3 cite it directly.
0 of 45 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K142060: Transom Anterior Cervical Plate, Neurostructures, Inc. (2014) Summary page 4.

## Most influential descendants
- K202064: Admiral ACP System (2020), 14 descendants of its own
- K211903: Shoreline Threaded TruProfile® Plate (2021), 7 descendants of its own
- K212139: Admiral ACP System (2021), 6 descendants of its own
- K233640: Segmental Plating System (SPS);IdentiTi SPS Interbody System;IdentiTi NanoTec SPS Interbody System; Transcend SPS Interbody System;Transcend NanoTec SPS Interbody System (2024), 5 descendants of its own
- K252611: aprevo® cervical plating system (2025), 3 descendants of its own

## Indications for use
The SeaSpine Cabo ACP (Anterior Cervical Plate) System is intended for anterior cervical fixation (C2-T1) 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, * Trauma (i.e., fracture or dislocation), * Spinal Stenosis, * Deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), * Tumor, * Pseudoarthrosis, » and failed previous fusion

Source page: https://510kreport.com/device/K173521
Methodology: https://510kreport.com/methodology