# K113781: Pantheon Spinal Ibfd System

- Pathway: 510(k) (Traditional)
- Applicant: Pantheon Spinal
- Decided: Apr 26, 2013 after 491 days
- Product code: MAX (Intervertebral Fusion Device With Bone Graft, Lumbar)
- Device class: 2
- Regulation: 21 CFR 888.3080
- 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
- K181548: Pantheon Spinal Pontus Interbody Fusion Device (2019), 1 descendant of its own
- K203003: Pantheon IBFD (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K113781
Methodology: https://510kreport.com/methodology