# K100180: Surgiquest Anchorport Sil Kit

- Pathway: 510(k) (Traditional)
- Applicant: Surgiquest, Inc.
- Decided: May 5, 2010 after 104 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). 32 ancestors in all.
No later device cites it as a predicate yet.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063859: Surgiquest Elastomeric Optical Trocar & Cannula, Surgiquest, Inc. (2007) Summary page 1.
- K090275: Gelport Single Incision Access System, Applied Medical Resources Corp. (2009) Summary page 1.
- K082619: Sils Port, Models SILSPT5, SILSPT12, Covidien Lp, Formerly Registered AS United States (2008) Summary page 1.
- K903419: Modified Surgiport Disposable Trocar and Sleeve, United States Surgical, A Division of Tyco Healthc (1990) Summary page 1.
- K032676: Endopath Bladeless Trocar, Endopath Blunt Tip Trocar, Endopath Dilating Tip Trocar, Ethicon Endo-Surgery, Inc. (2003) Summary page 1.

## Indications for use
The AnchorPort® SIL Kit has applications in abdominal minimally invasive surgical procedures and specifically where the surgeon will make a single skin incision in order to facilitate the use of multiple trocars to establish a port of entry for operating endoscopic instruments.

Source page: https://510kreport.com/device/K100180
Methodology: https://510kreport.com/methodology