# K262149: corra® cervical plating system

- Pathway: 510(k) (Traditional)
- Applicant: Carlsmed, Inc.
- Decided: Sep 24, 2026 after 91 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: 13 generations back to K922087 (1992). 61 ancestors in all.
No later device cites it as a predicate yet.
0 of 62 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K260570: corra™ cervical plating system, Carlsmed, Inc. (2026) Summary page 5.

## Indications for use
The corra® cervical plating 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. The corra® cervical plating system is intended to be used in conjunction with the aprevo® cervical interbody, system.

Source page: https://510kreport.com/device/K262149
Methodology: https://510kreport.com/methodology