# K002592: Interpore Cross Anterior Cervical Plate System

- Pathway: 510(k) (Traditional)
- Applicant: Interpore Cross Intl.
- Decided: Oct 6, 2000 after 46 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.
88 later devices descend from it; 2 cite it directly.
0 of 89 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K040844: Life Spine Neo Anterior Cervical Plate System (2004), 77 descendants of its own
- K070285: Life Spine Anterior Cervical Plate System (2007), 57 descendants of its own
- K062643: Kinetic Anterior Cervical Plate (2006), 53 descendants of its own
- K073479: Kinetic-SL Anterior Cervical Plate System (2008), 52 descendants of its own
- K100614: Hallmark Anterior Cervcial Plate System, Hallmark Five-Level Cervical Plates (2010), 51 descendants of its own

Source page: https://510kreport.com/device/K002592
Methodology: https://510kreport.com/methodology