# K913561: Luque Segmental Spinal Instrumentation

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer, Inc.
- Decided: Jan 16, 1992 after 160 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.
45 later devices descend from it; 1 cites it directly.
0 of 46 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K110348: Universal Clamp Spinal Fixation System (2011), 44 descendants of its own
- K121541: Jazz System (2012), 27 descendants of its own
- K142053: Universal Clamp Spinal Fixation System (2014), 23 descendants of its own
- K132395: Ligapass (2013), 23 descendants of its own
- K132287: Jazz System (2013), 15 descendants of its own

Source page: https://510kreport.com/device/K913561
Methodology: https://510kreport.com/methodology