# K181852: Percuvance Percutaneous Surgical System

- Pathway: 510(k) (Traditional)
- Applicant: Teleflexmedical, Inc.
- Decided: Oct 12, 2018 after 93 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K912544 (1991). 23 ancestors in all.
No later device cites it as a predicate yet.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K153063: Percuvance  Percutaneous Surgical System, Teleflexmedical, Inc. (2016) Summary page 7.
- K133202: Hem-O-Lok Ligating Clip, Teleflex Medical (2013) Summary page 7.

## Indications for use
The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok® ligating clips to soft tissue during laparoscopic surgery.

Source page: https://510kreport.com/device/K181852
Methodology: https://510kreport.com/methodology