# K130121: Short Port Blunt Tip Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific Corporation
- Decided: Apr 11, 2013 after 84 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 K992353 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992353: Blunt Tip Trocar Port, Origin Medsystems, Inc. (1999) Summary page 1.

## Indications for use
This product has applications for surgery in the saphenous vein, or radial artery for establishment of a port of entry for endloscopic instruments.

Source page: https://510kreport.com/device/K130121
Methodology: https://510kreport.com/methodology