# K071372: Modification to: Interplate VBR System

- Pathway: 510(k) (Special)
- Applicant: Rsb Spine, LLC
- Decided: Jun 11, 2007 after 26 days
- Product code: MQP (Spinal Vertebral Body Replacement Device)
- 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.
No later device cites it as a predicate yet.
0 of 1 device 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) InterPlate VBR: named in the summary without a submission number

## Indications for use
The InterPlateTM GC VBR device is indicated for the replacement of a complete or partial vertebrectomy, when used with a bone graft to facilitate fusion. It is designed to restore biomechanical integrity of the thoracic and lumbar spine, from TI to L5, which has been damaged due to a collapsed or unstable vertebral body resulting from a tumor or traumatic injury.

Source page: https://510kreport.com/device/K071372
Methodology: https://510kreport.com/methodology