# K010989: Telescopic Plate Spacer Thoracolumbar (TPS-TL) Spinal, Model 8119, 8120, 8130, 8131

- Pathway: 510(k) (Traditional)
- Applicant: Interpore Cross Intl.
- Decided: Nov 7, 2001 after 218 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K020204: Telescopic Plate Spacer Thoracolumbar (TPS-TL) Spinal System, Models 8123, 8124, 8132, 8133, 8156, 8157, 8158, & 8189 (2002), 0 descendants of its own
- K014145: Modification to Telescopic Plate Spacer Thoracolumbar (TPS-TL) Spinal System, Model 8130, 8131 (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K010989
Methodology: https://510kreport.com/methodology