# K032607: Powerpro Pneumatic System, Models PRO6150, PRO6175, PRO6185

- Pathway: 510(k) (Traditional)
- Applicant: Linvatec Corp.
- Decided: Nov 10, 2003 after 77 days
- Product code: DZI (Drill, Bone, Powered)
- Device class: 2
- Regulation: 21 CFR 872.4120
- 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 K832187 (1983). 2 ancestors in all.
6 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K832187: Hall Oscillator, Amsco Co. (1983) Summary page 2.
- K020069: Medtronic Mida Rex Legend System, Midas Rex Legend Pneumatic High Speed System or Legend System, Medtronic Midas Rex (2002)

## Cited in the summary but kept off the family tree
- K981269: Universal Drive System, Linvatec Corp. (1998). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Most influential descendants
- K062842: Twist Drill (2006), 5 descendants of its own
- K213072: 2.1 x 255mm Drill, 22mm Stop (2022), 1 descendant of its own
- K223199: 2.1 x 255mm Drill, 22mm Stop (2022), 0 descendants of its own
- K213208: Twist Drills (2021), 0 descendants of its own
- K170442: Cranial Drill Bits and Accessories (2017), 0 descendants of its own

## Indications for use
The PowerPro@ Pneumatic System consists of handpieces and attachments intended to be used for cutting, drilling, tapping, reaming, and driving screws and pins in large and small bone during orthopedic, spinal, neurosurgical, medial sternotomy, and oral and maxillofacial procedures.

Source page: https://510kreport.com/device/K032607
Methodology: https://510kreport.com/methodology