# K130758: Kronner Side-Kick Uterine Manipulator Holder

- Pathway: 510(k) (Traditional)
- Applicant: Kronner Prototypes, Inc.
- Decided: Dec 11, 2013 after 266 days
- Product code: LKF (Cannula, Manipulator/Injector, Uterine)
- Device class: 2
- Regulation: 21 CFR 884.4530
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K941458 (1995). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071405: Probe Holder System, Intuitive Surgical, Inc. (2007) Summary page 2.

## Indications for use
For holding Uterine manipulators during laparoscopic or open surgery on female pelvic organs.

Source page: https://510kreport.com/device/K130758
Methodology: https://510kreport.com/methodology