# K860158: 8-Channel Multiprog Implant Spinal Cord Stimulator

- Pathway: 510(k) (Traditional)
- Applicant: Neuromed, Inc.
- Decided: Mar 7, 1986 after 50 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K960728: One Step Connect Leads (Quattrode, Octrode, Cervitrode) (1996), 3 descendants of its own
- K991784: Renew Lead Extension (1999), 1 descendant of its own
- K992946: Renew Receiver (1999), 0 descendants of its own
- K990469: Lamitrode Leads (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K860158
Methodology: https://510kreport.com/methodology