# K112361: Alamo C

- Pathway: 510(k) (Traditional)
- Applicant: Alliance Partners, LLC
- Decided: Nov 30, 2011 after 105 days
- Product code: ODP (Intervertebral Fusion Device With Bone Graft, Cervical)
- 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.
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
- K133321: Alamo C (2014), 3 descendants of its own
- K173128: Alamo® C (2018), 2 descendants of its own
- K252737: DeGen Medical Latitude-C AM Cervical Interbody Fusion System (2025), 0 descendants of its own
- K213115: CHENA-C Spacer System (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K112361
Methodology: https://510kreport.com/methodology