# K093372: Sils Port Model SILSPT15

- Pathway: 510(k) (Special)
- Applicant: Covidien Lp, Formerly Registered AS Tyco Healthcar
- Decided: Dec 3, 2009 after 35 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: 5 generations back to K940232 (1994). 24 ancestors in all.
9 later devices descend from it; 3 cite it directly.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082619: Sils Port, Models SILSPT5, SILSPT12, Covidien Lp, Formerly Registered AS United States (2008) Summary page 1.
- K981941: Multaport Cannula Reducer and Accessories, Dexide, Inc. (1998) Summary page 1.

## Most influential descendants
- K103253: Sils Port (2011), 4 descendants of its own
- K141715: Glove Port (2015), 3 descendants of its own
- K110792: Gelpoint Path (2011), 3 descendants of its own
- K133393: Gelpoint Path Transanal Access Platform (2014), 1 descendant of its own
- K233263: Disposable Trocars (2024), 0 descendants of its own

## Indications for use
The SILS Port is indicated for multiple instrument or camera access to the abdominal cavity through a single incision for performing minimally invasive laparoscopic procedures.

Source page: https://510kreport.com/device/K093372
Methodology: https://510kreport.com/methodology