# K070891: Altiva Classic Acp System

- Pathway: 510(k) (Traditional)
- Applicant: Altiva Corp.
- Decided: Jun 11, 2007 after 73 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.
12 later devices descend from it; 2 cite it directly.
0 of 13 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
- K143576: Exactech Ambassador (2015), 7 descendants of its own
- K190227: Boomerang™ Anterior Cervical Plate System (2019), 4 descendants of its own
- K122216: Reliance Anterior Cervical Plate System (2012), 3 descendants of its own
- K243015: Skyway Anterior Cervical Plate System (2024), 2 descendants of its own
- K140742: Reliance Anterior Cervical Plate (2014), 2 descendants of its own

## Indications for use
The Altiva Classic ACP System is intended for anterior screw fixation to the cervical spine (C2 to C7). The system is intended for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with: * degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), * spondylolisthesis, * trauma (i.e. fractures or dislocations), * tumors, * deformity (defined by kyphosis, lordosis, or scoliosis), * pseudoarthrosis, and * failed previous fusion.

Source page: https://510kreport.com/device/K070891
Methodology: https://510kreport.com/methodology