# K162070: Joinix Cannular System

- Pathway: 510(k) (Traditional)
- Applicant: Aju Pharm Co., Ltd.
- Decided: Mar 16, 2017 after 232 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
Longest line of descent: 1 generation back to K920454 (1992). 1 ancestor in all.
1 later device descends 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)
- K920454: Cleartrac Cannula, Acufex Microsurgical, Inc. (1992) Summary page 4.

## Most influential descendants
- K212912: OneFix Biocomposite Anchors, OneFix Biocomposite Small Anchors, OneFix All Suture Anchors, OneFix Interference Screws, OneFix Cannula System (2021), 0 descendants of its own

## Indications for use
For introduction of instrumentation through a portal for surgical procedure.

Source page: https://510kreport.com/device/K162070
Methodology: https://510kreport.com/methodology