# K170084: InterLock Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Fujifilm New Development U.S.A., Inc.
- Decided: Mar 10, 2017 after 59 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K990028 (1999). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060096: Modular Trocar System, Applied Medical Resources Corp. (2006) Summary page 4.

## Indications for use
The InterLock Trocar has applications in abdominal, thoracic, and gynecological minimally invasive surgical procedures to establish a path of entry for endoscopic instruments. The trocar may be used with or without visualization for primary and secondary insertions.

Source page: https://510kreport.com/device/K170084
Methodology: https://510kreport.com/methodology