# K934779: Agram Spyral Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Agram Export-Import Co.
- Decided: Mar 14, 1995 after 524 days
- Product code: GXZ (Electrode, Needle)
- Device class: 2
- Regulation: 21 CFR 882.1350
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
14 later devices descend from it; 1 cites it directly.
0 of 15 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
- K050194: Axon Systems Subdermal Needle Electrodes (2005), 13 descendants of its own
- K073229: Nerve Monitoring Cable (2008), 5 descendants of its own
- K072276: Subdermal Needle Electrodes (2008), 5 descendants of its own
- K142438: Nerve Monitoring Cable System (2015), 4 descendants of its own
- K182617: ATEC IOM Accessory Instruments (2019), 3 descendants of its own

Source page: https://510kreport.com/device/K934779
Methodology: https://510kreport.com/methodology