# K943694: Ebi Anterior Cervical Spine System

- Pathway: 510(k) (Traditional)
- Applicant: Electro-Biology, Inc.
- Decided: Feb 8, 1995 after 194 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K043082: The Tosca Anterior Cervical Plate System (2004), 3 descendants of its own
- K153042: TRYPTIK2C-plate Anterior Cervical Plate System (2016), 1 descendant of its own
- K171797: TRYPTIK2 C-Plate Anterior Cervical Plate System (2018), 0 descendants of its own
- K132310: ASCOT (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K943694
Methodology: https://510kreport.com/methodology