# K060274: Piezotome

- Pathway: 510(k) (Traditional)
- Applicant: Satelec
- Decided: May 1, 2006 after 88 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: 2 generations back to K042434 (2004). 2 ancestors in all.
10 later devices descend from it; 3 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K043408: Piezosurgery Device, Piezosurgery S.R.L. (2005) Summary page 1.

## Most influential descendants
- K072146: Ems Piezon Master Surgery (2007), 6 descendants of its own
- K121620: Ultrasonic Surgery (2012), 2 descendants of its own
- K113152: Ultrasonic Surgery Machine (2012), 2 descendants of its own
- K151171: Traus SUS10 (2015), 1 descendant of its own
- K091331: Piezotome 2 (2009), 1 descendant of its own

## Indications for use
The PiezotomeTM device is a bone cutting instrument intended for use in oral surgery.

Source page: https://510kreport.com/device/K060274
Methodology: https://510kreport.com/methodology