# K062209: Basx Bladeless Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Ethicon Endo-Surgery, LLC
- Decided: Oct 10, 2006 after 70 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
No predicates in its family tree.
70 later devices descend from it; 1 cites it directly.
0 of 71 devices 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) ENDOPATH® Optiview Optical Surgical Obturator and Sleeve: named in the summary without a submission number
- (no number) ENDOPATH® Non-Bladed Solid Obturator (with Sleeve): named in the summary without a submission number
- (no number) ENDOPTH® XCEL TM Bladeless Trocar: named in the summary without a submission number

## Most influential descendants
- K070158: R-Port Laparoscopic Access Device (2007), 69 descendants of its own
- K073170: R-Port II Laparoscopic Access Device (2007), 68 descendants of its own
- K082619: Sils Port, Models SILSPT5, SILSPT12 (2008), 58 descendants of its own
- K090902: Spider Single Port Surgical Device, Support Arm Accessory,  Model 90001, 90002, 90003 (2009), 46 descendants of its own
- K112208: Intutive Surgical DA Vinci Single Site Instruments and Accessories (2011), 43 descendants of its own

## Indications for use
The BASXTM Bladeless Trocar has applications in abdominal and gynecologic minimally invasive surgical procedures to establish a path of entry for endoscopic instruments.

Source page: https://510kreport.com/device/K062209
Methodology: https://510kreport.com/methodology