# K001372: E-Z Link Cross Connector

- Pathway: 510(k) (Traditional)
- Applicant: Depuyacromed
- Decided: Jul 27, 2000 after 87 days
- Product code: KWP (Appliance, Fixation, Spinal Interlaminal)
- Device class: 2
- Regulation: 21 CFR 888.3050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
190 later devices descend from it; 5 cite it directly.
0 of 191 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
- K013296: Moss Miami Spinal Systems (2001), 184 descendants of its own
- K092825: Apex Spine System 5.50 MM Titanium Rod & Polyaxial Screw Washer (2010), 178 descendants of its own
- K102488: Apex Spine System W/ Cocr Rods (2010), 177 descendants of its own
- K120270: Venus Spinal Fixation System (2012), 111 descendants of its own
- K110906: Apex Spine System (2011), 103 descendants of its own

Source page: https://510kreport.com/device/K001372
Methodology: https://510kreport.com/methodology