# K092659: Spinal Usa RCS Anterior Lumbar Butress Plate System, Model 22-1001-25

- Pathway: 510(k) (Traditional)
- Applicant: Spinal USA
- Decided: Nov 17, 2009 after 81 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.
50 later devices descend from it; 4 cite it directly.
0 of 51 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
- K142699: LITe Plate System (2014), 46 descendants of its own
- K150449: LITe Plate System (2015), 24 descendants of its own
- K190016: Lateral Plate System (2019), 15 descendants of its own
- K192481: AccelFix Lumbar Plate System (2020), 13 descendants of its own
- K210035: ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System (2021), 10 descendants of its own

## Indications for use
The Spinal USA RCS Anterior Buttress Plate System is intended to stabilize the allograft or autograft at on level (TI-S1) as an aid to spinal fusion and to provide temporary stabilization and augment development of a solid spinal fusion. It may be used alone or with other anterior, anterolateral, or posterior spinal systems made of compatible materials. The device is not intended for load bearing applications.

Source page: https://510kreport.com/device/K092659
Methodology: https://510kreport.com/methodology