# K072811: Marionette SA, Model 001 001 & 001 002

- Pathway: 510(k) (Traditional)
- Applicant: Kinetic Surgical, LLC
- Decided: Apr 21, 2008 after 203 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: 3 generations back to K910831 (1991). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043541: Endolink True Movement System, Novare Surgical Systems, Inc. (2005) Summary page 1.
- K962119: RE-New Laparoscopic Instruments, Microline Pentax, Inc. (1996) Summary page 1.
- K061425: Purewrist Scissors, Model PW1101-01;Purewrist Dissector,  Model PW1201-01;Purewrist Hook, Model PW1301-01, Cambridge Endoscopic Devices (2006) Summary page 1.

## Indications for use
The MarionetteTM SA is intended for use by surgeons for grasping, dissection, tissue cutting during laparoscopic surgical procedures.

Source page: https://510kreport.com/device/K072811
Methodology: https://510kreport.com/methodology