# K001597: Conmed Trogard Finesse Trocar System, Model 60-6050-XXX

- Pathway: 510(k) (Special)
- Applicant: Conmedcorp
- Decided: Jun 5, 2000 after 13 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
No predicates in its family tree.
2 later devices descend 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K073009: Oneport Surgical Trocar System (2007), 1 descendant of its own
- K142464: Entriport (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K001597
Methodology: https://510kreport.com/methodology