# K073009: Oneport Surgical Trocar System

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Corporation
- Decided: Dec 7, 2007 after 43 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: 1 generation back to K924761 (1993). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K924761: Sterile Endoscopic Dispos Trocars W/Safe Shield, Richard-Allan Medical Ind., Inc. (1993) Summary page 1.
- K933456: Comed Trogard (TM) Blunt Tip Trocar/Sleeve, Conmedcorp (1993) Summary page 1.
- K952977: Sabre Multi-Use Trocar System, Endoscopic Concepts, Inc. (1995) Summary page 1.
- K001597: Conmed Trogard Finesse Trocar System, Model 60-6050-XXX, Conmedcorp (2000). Our reading of the summary gave K001697, which is not a number in FDA’s lists. Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “ConMed TroGARD Finesse Trocar System”.

## Most influential descendants
- K142464: Entriport (2015), 0 descendants of its own

## Indications for use
The CONMED OnePort® Surgical Trocar System has applications in a variety of endoscopic procedures to provide a means of abdominal entry and access for endoscopic instruments.

Source page: https://510kreport.com/device/K073009
Methodology: https://510kreport.com/methodology