# K073232: Indus Anterior Cervical Plate System, Model IM3XXX

- Pathway: 510(k) (Traditional)
- Applicant: Spinefrontier, Inc.
- Decided: Feb 20, 2008 after 97 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: 1 generation back to K030866 (2003). 1 ancestor in all.
17 later devices descend from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030866: Synthes Anterior CSLP System, Synthes (Usa) (2003) Summary page 1.

## Most influential descendants
- K093776: Indus Anterior Cervical Plate System (2010), 16 descendants of its own
- K121060: Spine Frontier Indus Acp System (2012), 15 descendants of its own
- K153526: Pyrenees Cervical Plate System (2016), 6 descendants of its own
- K140234: Aspiron Acp System (2014), 6 descendants of its own
- K162664: Pyrenees Cervical Plate System (2016), 5 descendants of its own

## Indications for use
The INDUSTM Anterior Cervical Plate System is intended for anterior cervical intervertebral body fixation. This system is indicated for patients in whom stability is desired following anterior cervical fusion. The levels of treatment range from C2 to C7. Indications include symptomatic cervical spondylolisthesis, trauma (fracture or dislocation), spinal stenosis, deformities or curvatures (scoliosis, kyphosis and or lordosis), tumor, pseudoarthrosis, degenerative disc disease (defined as discogenic pain with degeneration of the disc confirmed by history and radiographic studies), and re-operation for failed fusion or instability following surgery for above indications.

Source page: https://510kreport.com/device/K073232
Methodology: https://510kreport.com/methodology