# K143191: IntelliSense Drill

- Pathway: 510(k) (Traditional)
- Applicant: Mcginley Innovations
- Decided: Feb 20, 2015 after 106 days
- Product code: HWE (Instrument, Surgical, Orthopedic, Ac-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 K943589 (1994). 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)
- K943589: Stryker Total Performance System, Stryker Corp. (1994) Summary page 4.

## Most influential descendants
- K200575: Truemed Hand, Foot and Ankle Plates System (2021), 0 descendants of its own

## Indications for use
The IntelliSense Drill is intended to bore a hole into bone for insertion of a screw, wire, cable, plate, pin, bolt, etc. In Bicortical mode, the IntelliSense Drill is indicated to be used in bicortical long bone, such as the femur, tibia, fibula, humerus, ulna, and radius.

Source page: https://510kreport.com/device/K143191
Methodology: https://510kreport.com/methodology