# K023133: Modification to Ebi Vuelock Anterior Cervical Plate System

- Pathway: 510(k) (Special)
- Applicant: Ebi, L.P.
- Decided: Oct 18, 2002 after 28 days
- Product code: KWQ (Appliance, Fixation, Spinal Intervertebral Body)
- Device class: 2
- Regulation: 21 CFR 888.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 5 cite it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) EBI VueLockTM Anterior Cervical Plate System: named in the summary without a submission number

## Most influential descendants
- K051815: Modification to Vertebron SCP Cervical Plate System (2005), 10 descendants of its own
- K062110: Vertebron SCP Cervical Plate System (2006), 9 descendants of its own
- K081567: Vertebron SSP Cervical Plating System (2008), 6 descendants of its own
- K172104: Ozark (tm) Cervical Plate System (2017), 5 descendants of its own
- K191500: NuVasive® ACP System (2019), 4 descendants of its own

## Indications for use
The EBI VueLockTM Anterior Cervical Plate System is intended for anterior interbody screw fixation of the cervical spine. The System is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusions in patients with degenerative disc disease (as defined by neck pain of discogenic origin of the disc confirmed by patient history and radiographic studies), trauma (including fractures), tumors, deformity (defined as kyphosis, lordosis, or scoliosis), pseudarthrosis, andor failed previous fusions.

Source page: https://510kreport.com/device/K023133
Methodology: https://510kreport.com/methodology