# K930242: Introde Int-8

- Pathway: 510(k) (Traditional)
- Applicant: Neuromed, Inc.
- Decided: Feb 2, 1994 after 379 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K994097: Medamicus Epidural Introducer (2000), 1 descendant of its own
- K013120: Percutaneous Introducer Set, Model 042294 and Kit Model 3550-18 (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K930242
Methodology: https://510kreport.com/methodology