# K063746: Power Extenders Model# PEC200, PES200,PES200S

- Pathway: 510(k) (Special)
- Applicant: Power Medical Interventions, Inc.
- Decided: Jan 12, 2007 after 25 days
- Product code: GDW (Staple, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K970720 (1997). 26 ancestors in all.
13 later devices descend from it; 2 cite it directly.
0 of 40 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052415: Power Linear Cutter Reusable Digital Loading Units with Reloads, Power Medical Interventions, Inc. (2005) Summary page 1.

## Most influential descendants
- K073001: Idrives, Idrivec, Idrivef (2007), 11 descendants of its own
- K102325: Idrive System (I Drive Power Handle, Idrive (Ralc) Single Use Reload) (2010), 9 descendants of its own
- K121510: Idrive Ultra Powered Handle Endo Gia Adapter (2012), 8 descendants of its own
- K160176: Signia Stapler (2016), 5 descendants of its own
- K202864: Tri-Staple 2.0 Reloads (2020), 1 descendant of its own

## Indications for use
The Power Extenders have applications for general and endoscopic surgery in gastrointestinal, gynecological, general abdominal, and thoracic surgical procedures for resection, transection, creation of anastomoses, and for open occlusion of the hear's left atrial appendage.

Source page: https://510kreport.com/device/K063746
Methodology: https://510kreport.com/methodology