# K152282: Cam Lock Plating System

- Pathway: 510(k) (Traditional)
- Applicant: Life Spine, Inc.
- Decided: Nov 20, 2015 after 100 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: 5 generations back to K926453 (1993). 24 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070285: Life Spine Anterior Cervical Plate System, Life Spine (2007) Summary page 4.
- K070775: Modification to: Providence Anterior Cervical Plate System, Globus Medical, Inc. (2007) Summary page 4.
- K130202: Iris Anterior Cervical Plate, Life Spine, Inc. (2013) Summary page 4.

## Most influential descendants
- K243369: Cervical Plating System (2024), 0 descendants of its own

## Indications for use
This system is intended for anterior interbody screw fixation of the cervical spine. The system is indicated for use in the temporary stabilization of the anterior spine from C2 to T1 during the development of cervical spinal fusions in patients with: 1.) Degenerative disc disease, DDD (as defined by neck pain of discogenic origin with degeneration of disc confirmed by patient history and radiographic studies); 2). Spondylolisthesis; 3.) Trauma (including fractures or dislocations); 4.) Spinal cord stenosis; 5.) Deformity or curvatures (i.e. kyphosis, lordosis or scoliosis); 6.) Tumors; 7.) Pseudarthrosis; and/or 8.) Failed previous fusions. Nota Bene: This device system is intended for anterior cervical interverterbral body fusions only.

Source page: https://510kreport.com/device/K152282
Methodology: https://510kreport.com/methodology