# K033249: Pajunk Modular Handle Instruments

- Pathway: 510(k) (Traditional)
- Applicant: Pajunk GmbH
- Decided: Mar 5, 2004 after 150 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: 1 generation back to K935270 (1994). 1 ancestor in all.
14 later devices descend from it; 5 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K935270: Modular Forcep and Scissor System, Richard Wolf Medical Instruments Corp. (1994) Summary page 1.

## Most influential descendants
- K102921: Endoscopic Monopolar Instruments and Accessories (2011), 4 descendants of its own
- K053282: Adaptable Monopolar Electrodes with Ceramic Tip (2005), 3 descendants of its own
- K062047: Adaptable Monopolar Adaptable and/or Retractable Electrodes (2006), 2 descendants of its own
- K062072: Pajunks Disposable Inserts for Handle Instruments and HF Electrodes (2006), 2 descendants of its own
- K171825: Disposable Endoscopic Surgical Instrument, Reusable Endoscopic Surgical Instrument (2018), 1 descendant of its own

## Indications for use
Instruments insulated for optional monopolar coagulation which enable a surgeon to grasp, manipulate, dissect, retrieve, biopsy, cut or coagulate internal tissue or organs while performing laparoscopic procedures.

Source page: https://510kreport.com/device/K033249
Methodology: https://510kreport.com/methodology