# K072840: Endius Title 2 Polyaxial Spinal System

- Pathway: 510(k) (Traditional)
- Applicant: Endius, Inc.
- Decided: Dec 7, 2007 after 64 days
- Product code: NKB (Thoracolumbosacral Pedicle Screw System)
- Device class: 2
- Regulation: 21 CFR 888.3070
- 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; 2 cite 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
- K073510: Endius Title 2 Poly Axial Spinal System (2008), 3 descendants of its own
- K133086: Title 2 Polyaxial Spinal System (2013), 1 descendant of its own
- K142752: Minit Posterior Cervical-Thoracic Fixation System, Nex-Link Spinal Fixation System, Nex-Link OCT Cervical Plating System, Sequoia Pedicle Screw System including SpeedLink II, ST360º Spinal Fixatoin System, Title 2 Polyaxial Spinal System (2015), 0 descendants of its own
- K122592: Instinct Java System (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K072840
Methodology: https://510kreport.com/methodology