# K990104: Medtronic Model 7495 Extension Kit

- Pathway: 510(k) (Special)
- Applicant: Medtronic Vascular
- Decided: Feb 9, 1999 after 28 days
- Product code: GZB (Stimulator, Spinal-Cord, Implanted (Pain Relief))
- Device class: 2
- Regulation: 21 CFR 882.5880
- 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) Medtronic Model 7495 extension kit: named in the summary without a submission number

## Indications for use
The Medtronic Model 7495 Extension Kit is intended for use with implanted spinal cord or peripheral nerve stimulation systems for the treatment of chronic, intractable pain.

Source page: https://510kreport.com/device/K990104
Methodology: https://510kreport.com/methodology