# K112599: Insurgical Single Use Power Equipment

- Pathway: 510(k) (Traditional)
- Applicant: Insurgical, LLC
- Decided: Nov 6, 2012 after 426 days
- Product code: KIJ (Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment)
- Device class: 1
- Regulation: 21 CFR 878.4820
- 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 K972367 (1997). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972367: Stryker System 4000 Heavy Duty Battery Powered Equipment, Stryker Instruments (1997) Summary page 3.

## Most influential descendants
- K240071: Peleton Universal Single Use Power System and Attachments (2024), 0 descendants of its own

## Indications for use
InsurgicalTM Single Use Power Equipment is intended for use in the cutting, drilling, decorticating, and smoothing of bone and other bone related tissue in a variety of surgical procedures. It is also usable in the placement or cutting of screws, wires, pins, and other fixation devices. It can also be used to cut metal.

Source page: https://510kreport.com/device/K112599
Methodology: https://510kreport.com/methodology