# K122801: Providence Cervical Cage

- Pathway: 510(k) (Traditional)
- Applicant: Providence Medical Technology, Inc.
- Decided: May 24, 2013 after 253 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: 11 generations back to K841189 (1984). 50 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 52 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- P980048: Bak/Cervical (Bak/C) Interbody Fusion System, Sulzer Spine-Tech (2001) Summary page 1.
- K111123: Varilift Cervical Interbody Fusion System, Wenzel Spine (2011) Summary page 1.
- K092070: Interplate C, Rsb Spine, LLC (2009) Summary page 1.
- K082848: Nubic and Rabea Devices, Signus Medizintechnik GmbH (2009) Summary page 1.
- K121320: C7 Anterior Cervical Intervertebral Fusion Cage, Medyssey Co, Ltd. (2012) Summary page 1.

## Most influential descendants
- K161642: CAVUX™ Cervical Cage (2016), 0 descendants of its own

## Indications for use
PMT Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DOD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. ODD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system.

Source page: https://510kreport.com/device/K122801
Methodology: https://510kreport.com/methodology