# K062371: Preview Anterior Cervical Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Alphaspine, Inc.
- Decided: Dec 4, 2006 after 112 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K223627: PreView-III™ Anterior Cervical Plate System (2023), 1 descendant of its own
- K261279: DeltaNEC Interbody System (2026), 0 descendants of its own
- K073500: Active Anterior Cervical Plate System (2008), 0 descendants of its own

## Indications for use
The PreView Tm Anterior Cervical Plate System is intended for the treatment of the cervical spine in skeletally mature patients receiving fusion by autogenous and/or allogenic bone graft, The implants are attached to the anterior cervical spine (C2-Tl) with remhoval of the implants after the attainment of a solid fusion mass. The PreView TM Anterior Cervical Plate System is intended for use under the following indications: * Degenerative disc disease (DDD) (defined as neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies) * Spondylolisthesis : Trauma (i.e., fracture or dislocation) · Spinal stenosis 1Deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis) * Tumor *Pseudoarthrosis * Failed previous fusion

Source page: https://510kreport.com/device/K062371
Methodology: https://510kreport.com/methodology