# K133321: Alamo C

- Pathway: 510(k) (Special)
- Applicant: Alliance Partners, LLC
- Decided: Jan 9, 2014 after 72 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
Longest line of descent: 9 generations back to K841189 (1984). 19 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112361: Alamo C, Alliance Partners, LLC (2011)
- K081917: Depuy Spine Bengal, Concorde, Cougar, Devex and Leopard Systems, Depuy Spine, Inc. (2009) Summary page 1.
- K081730: Novel Cervical Spinal Spacer System, Alphatec Spine, Inc. (2008) Summary page 1.

## Most influential descendants
- 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

## Indications for use
The Alamo C is indicated for anterior cervical interbody fusion procedures in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one level from C2-T1. DDD is defined as discogenic pain with the degeneration of the disc confirmed by history and radiographic studies. These patients should have had six weeks of non-operative treatment prior to treatment with an intervertebral cage. The device system must be used with supplemental fixation and autograft to facilitate fusion and is to be implanted via an open, anterior approach.

Source page: https://510kreport.com/device/K133321
Methodology: https://510kreport.com/methodology