# K093783: Innovia Innoport Laparoscopic Access Port

- Pathway: 510(k) (Traditional)
- Applicant: Innovia, LLC
- Decided: Aug 23, 2010 after 257 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 K010007 (2001). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090677: Innoport Laparoscopic Access Device, Innovia, LLC (2009) Summary page 1.

## Indications for use
The Innovia InnoPort TMLaparoscopic Access Device is a sterile, single use device intended for use as a multiple instrument and/or camera port during minimally invasive laparoscopic abdominal surgery.

Source page: https://510kreport.com/device/K093783
Methodology: https://510kreport.com/methodology