# K013987: Reprocessed Disposable Trocars

- Pathway: 510(k) (Traditional)
- Applicant: Adven Medical
- Decided: Mar 1, 2002 after 87 days
- Product code: KBG (Trocar, Sinus)
- Device class: 1
- Regulation: 21 CFR 874.4420
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Disposable Trocars: named in the summary without a submission number

## Indications for use
Reprocessed endoscopic trocars are designed to provide a pathway for entry of minimally invasive instruments to a body organ or cavity during general, abdominal, thoracic, gynecologic or other minimally invasive surgical procedures. Trocars are single patient used devices.

Source page: https://510kreport.com/device/K013987
Methodology: https://510kreport.com/methodology