# K960082: Discography Kit

- Pathway: 510(k) (Traditional)
- Applicant: Spinal Specialties, Inc.
- Decided: Mar 21, 1996 after 70 days
- Product code: IZG (System, X-Ray, Photofluorographic)
- Device class: 2
- Regulation: 21 CFR 892.1730
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 3 cite it directly.
0 of 10 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
- K043500: Functional Anaesthetic Discography (Fad) System, Including Fad Catheter Kit and Fad Introducer Needle (2005), 3 descendants of its own
- K061210: Functional  Anaesthetic Discography (Fad) Catheter System, Model D01A ; Introducer Needle, Model D01B (2006), 2 descendants of its own
- K033739: Physician Industries' Durameter Syringe (2004), 2 descendants of its own
- K063071: Discyphor Catheter System, Model D01A; Discyphor Introducer Needle, Model D01B (2007), 1 descendant of its own
- K051136: Smith & Nephew CDS System (2005), 1 descendant of its own

Source page: https://510kreport.com/device/K960082
Methodology: https://510kreport.com/methodology