# K130306: Incite Anchored Cervical Interbody Device

- Pathway: 510(k) (Special)
- Applicant: Incite Innovation, LLC
- Decided: Apr 11, 2013 after 63 days
- Product code: OVE (Intervertebral Fusion Device With Integrated Fixation, 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: 11 generations back to K841189 (1984). 29 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122008: Incite Anchored Cervical Interbody (Aci) Fusion Device, Incite Innovation, LLC (2012) Summary page 1.

## Most influential descendants
- K150913: Incite Anchored Cervical Interbody Device (2015), 0 descendants of its own

## Indications for use
The Incite Anchored Cervical Interbody Device is indicated for use in skeletally mature patients with degenerative disc disease (DOD) of the cervical soine with accompanying radicular symptoms at one disc level from C2-TI. DDD is defined as discogenic pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six weeks of non-operative treatment. The Incite Anchored Cervical Interbody Device is to be used with autogenous bone graft and implanted via an open, anterior approach. Supplemental fixation, i.e. an anterior cervical plate, is required to properly utilize this system.

Source page: https://510kreport.com/device/K130306
Methodology: https://510kreport.com/methodology