# K912453: Intelijet TM Fluid Management System

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew Dyonics, Inc.
- Decided: Aug 26, 1991 after 84 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
95 later devices descend from it; 3 cite it directly.
0 of 96 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
- K971253: Various Arthroscopes, Endoscopic Blades, Manual Instruments (1997), 60 descendants of its own
- K043395: Smith & Nephew Videoarthroscope (2005), 32 descendants of its own
- K962114: Arthro-Surgimat (1996), 32 descendants of its own
- K983910: Arthro-Surgimat-1500 (1998), 31 descendants of its own
- K072879: Innervue Diagnostic Scope System (2008), 30 descendants of its own

Source page: https://510kreport.com/device/K912453
Methodology: https://510kreport.com/methodology