# K061155: Vista P Vertebral Body Replacement System

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer Trabecular
- Decided: Sep 22, 2006 after 149 days
- Product code: MQP (Spinal Vertebral Body Replacement Device)
- 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.
32 later devices descend from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K111983: Vista-S Device Model 08/06-401-Xxxxx, 08/06-402-Xxxxxx (2011), 31 descendants of its own
- K133784: Vista-S Device, Associated Instrumentation (2014), 29 descendants of its own
- K143297: Ardis Interbody System, BAK Interbody Fusion System, BAK/C Anterior Cervical Interbody Fusion System, InFix Anterior Lumbar System, TraXis Vertebral Body Replacement (Ti and VUE) (2015), 19 descendants of its own
- K162986: SPIRA Open Matrix ALIF (2017), 11 descendants of its own
- K180724: SPIRA Open Matrix LLIF (2018), 10 descendants of its own

## Indications for use
The Vista®P Vertebral Body Replacement System is a vertebral body replacement device intended for use in the thoracolumbar spine (Ti - L5) to replace a collapsed, damaged or unstable vertebral body due to tumor or traumw (i.e., fracture). The Viftat&P Vertebral Body Replacement is intended for use with supplemental internal spinal fixation systems. The Vista®P Vertebral Body Replacement may be used with bone graft.

Source page: https://510kreport.com/device/K061155
Methodology: https://510kreport.com/methodology